G B Rossi studies hereditary non-polyposis colorectal cancer (HNPCC), a genetic condition that increases the risk of developing colorectal cancer. He emphasizes the need for vigilant health monitoring among family members of those affected by HNPCC. Rossi's work involves examining how well these family members adhere to recommended health checks, like colonoscopies, which are crucial for early detection of cancer and other serious issues.
Key findings
In a study of 106 family members, only 40 participated in regular surveillance for colorectal cancer.
During the initial check-ups of those who participated, 7 cases of colorectal cancer and 14 polyps were found.
The study concluded that regular colonoscopies every two years significantly enhance the early detection of colorectal issues among HNPCC families.
Frequently asked questions
Does Dr. Rossi study hereditary non-polyposis colorectal cancer?
Yes, Dr. Rossi specifically studies hereditary non-polyposis colorectal cancer (HNPCC) and its impact on family health.
What treatments has Dr. Rossi researched?
Dr. Rossi's research focuses on monitoring techniques, particularly the effectiveness of regular colonoscopies in detecting early signs of cancer.
Is Dr. Rossi's work relevant to family members of cancer patients?
Yes, his work directly helps family members of HNPCC patients by promoting regular health surveillance and early cancer detection.
Publications in plain English
Molecular Basis of Adenomatous Gastrointestinal Polyposis Syndromes: Role of Pathogenic and Benign Variants in Disease Onset.
2026
Biomedicines
Cammarota F, D'Agostino V, Capasso C, Duraturo F, D'Angelo V +5 more
Plain English This study looked at genetic factors in people with adenomatous gastrointestinal polyposis syndromes, which can lead to tumors in the intestines. Researchers examined 60 patients suspected of having these syndromes and found that 55% had harmful genetic variants, while 18.3% had variants that are unclear in their significance. These findings matter because they help explain why some patients develop more polyps at an earlier age, highlighting the role of genetics in disease development.
Who this helps: This research benefits patients with gastrointestinal polyposis syndromes and their doctors, enabling better understanding and management of their conditions.
Plain English This study looked at how understanding patient attitudes and beliefs can help improve their acceptance of new medical treatments in interventional radiology, which are safer and less invasive. The research highlights that increasing awareness about these procedures can significantly boost their use among patients and doctors. By applying behavioral science theories, specifically how people feel about new technologies and their confidence in using them, healthcare can become more effective and patient-friendly.
Who this helps: Patients undergoing interventional radiology treatments.
[Corrigendum] Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures.
2025
International journal of oncology
Costabile V, Duraturo F, Delrio P, Rega D, Pace U +6 more
Plain English This paper discussed the effects of lithium chloride on colon cancer cells. The researchers found that lithium chloride can encourage cancer cells to change back into a more normal, epithelial-like state, which is a positive response because it may help reduce cancer progression. While the study's specific numerical results were not highlighted in this correction, the overall findings are important because they suggest a potential treatment method for colon cancer.
Who this helps: This helps patients with colon cancer.
Germline Variants in MLH1 and ATM Genes in a Young Patient with MSI-H in a Precancerous Colonic Lesion.
2023
International journal of molecular sciences
Nolano A, Rossi GB, D'Angelo V, Liccardo R, Rosa M +2 more
Plain English This study focuses on a 16-year-old boy who developed a precancerous lesion in his colon, raising concerns about Lynch syndrome, a genetic disorder linked to certain cancers. Researchers identified a change in the MLH1 gene that may increase cancer risk, along with two other uncertain genetic changes in the ATM gene. Understanding these genetic variations is crucial as it can help point to the combined effects that make young people like him more vulnerable to developing cancers in the future.
Who this helps: This helps patients at risk for Lynch syndrome and their doctors in diagnosing and managing their care.
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer.
2023
Cancers
Cecere F, Pignata L, Hay Mele B, Saadat A, D'Angelo E +9 more
Plain English This study examined a woman with Beckwith-Wiedemann Syndrome (BWS) who developed early-onset colorectal cancer (EO-CRC) at age 27. Researchers found genetic changes in her tumor, revealing a link between inherited mutations in the CFTR gene and other alterations that may influence cancer growth. This matters because understanding the genetic factors involved could help identify people at risk for early-onset colorectal cancer, potentially leading to earlier screenings and interventions.
Who this helps: This helps patients with BWS and their doctors in managing cancer risk.
Dynamic Compensation of a Piezoelectric Accelerometer Obtained through a General Probabilistic Approach.
2023
Sensors (Basel, Switzerland)
Crenna F, Rossi GB, Berardengo M
Plain English This study looked at improving how accurately an accelerometer measures movement by correcting for errors caused by its limitations. The researchers used a new approach that worked well in tests, showing that their method could significantly enhance measurement quality, especially when the actual movement signals are much stronger than background noise. This improvement matters because it can lead to more accurate data in dynamic situations, which is crucial for applications that rely on precise measurements.
Who this helps: This helps doctors and engineers who rely on accurate movement measurements in various technologies and medical devices.
Improvement in the Post-Processing of Wave Buoy Data Driven by the Needs of a National Coast and Sea Monitoring Agency.
2023
Sensors (Basel, Switzerland)
Rossi GB, Nardone G, Settanta G, Picone M, Berardengo M +1 more
Plain English This study focused on improving how data from ocean wave buoys is processed to better monitor sea conditions. Researchers tested two different methods for analyzing this data and found that the second method was more efficient and accurate, with an uncertainty of only a few degrees in predicting wave direction. This improvement could greatly enhance marine weather services, leading to better safety and efficiency for activities like shipping and fishing.
Who this helps: This benefits marine operators and coastal management agencies.
High-added value co-products obtained from pecan nut () using a green extraction technology.
2022
Journal of food science and technology
Polmann G, Rossi GB, Teixeira GL, Maciel LG, de Francisco A +3 more
Plain English This study looked at how to extract valuable products from pecan nuts using a green method that’s better for the environment. Researchers found that a specific enzyme treatment increased the nutrient quality of the extracted materials, yielding 726.3 mg of beneficial phenolic compounds per 100 grams, which is important for health. This finding is significant because it shows that pecan nut by-products can be used to create healthier food ingredients.
Who this helps: This benefits food manufacturers and health-conscious consumers.
A multicenter randomized phase 4 trial comparing sodium picosulphate plus magnesium citrate vs. polyethylene glycol plus ascorbic acid for bowel preparation before colonoscopy. The PRECOL trial.
2022
Frontiers in medicine
D'Angelo V, Piccirillo MC, Di Maio M, Gallo C, Bucci C +17 more
Plain English This study looked at two different solutions for cleaning out the bowels before a colonoscopy: one made of sodium picosulphate plus magnesium citrate (SPMC) and another made of polyethylene glycol plus ascorbic acid (PEG-ASC). Both preparations were similarly effective, with a success rate of 94.4% for PEG-ASC and 95.7% for SPMC. However, patients found SPMC easier to tolerate and were more willing to repeat the process compared to those using PEG-ASC, making SPMC a more comfortable option for bowel prep.
Who this helps: This benefits patients preparing for colonoscopies.
Investigation on Spectrum Estimation Methods for Bimodal Sea State Conditions.
2021
Sensors (Basel, Switzerland)
Rossi GB, Crenna F, Berardengo M, Piscopo V, Scamardella A
Plain English This study looked at two methods for estimating sea conditions using wave signals that combine wind and swell factors. The researchers found that different combinations of wave conditions affected how accurately each method worked; for example, they tested signals that lasted from 10 minutes to 1 hour. This matters because better estimation of sea conditions helps improve weather forecasting and ensures safer navigation for ships.
Who this helps: This research helps sailors and maritime navigation authorities.
Plain English This study looked at how to better estimate sea wave patterns using a mathematical model called ARMA. The researchers found that specific factors, such as the length of time data is collected and the number of data points used, significantly impact the accuracy of the wave estimations. By understanding these factors, the study offers clear recommendations to improve the reliability of sea wave predictions, which is crucial for navigating and managing marine activities.
Who this helps: This benefits scientists and engineers involved in maritime operations and coastal management.
Filtering Biomechanical Signals in Movement Analysis.
2021
Sensors (Basel, Switzerland)
Crenna F, Rossi GB, Berardengo M
Plain English This study examined different methods for improving the accuracy of biomechanical measurements, which are used to analyze how humans move. The researchers compared various filtering techniques to see which ones reduced errors in gathered data, ultimately suggesting that certain methods can better handle uncertainties in measurements. This matters because it helps ensure that the movement data used in healthcare and sports science is as precise as possible, which can lead to better assessments and treatments.
Who this helps: Patients, doctors, and sports professionals looking to understand human movement more accurately.
Rossi GB, Cannata A, Iengo A, Migliaccio M, Nardone G +2 more
Plain English This study looks at various methods used to measure sea waves, which are important for activities like weather forecasting, coastal safety, navigation, and harnessing renewable energy. It discusses techniques like buoys, satellites, and coastal radars, highlighting how they work, their current status, and future trends. The findings emphasize the need for better collaboration between these methods to improve overall monitoring.
Who this helps: This helps coastal communities, navigators, and energy developers.
Comparison of Spectrum Estimation Methods for the Accurate Evaluation of Sea State Parameters.
2020
Sensors (Basel, Switzerland)
Rossi GB, Crenna F, Piscopo V, Scamardella A
Plain English This study looked at different methods for analyzing ocean wave conditions, which is important for weather forecasting and ensuring ships can operate safely. It tested three methods and found that the Welch and Thomson techniques performed the best for accurately measuring key wave features, like the average height of waves and the average time between them. This matters because better analysis of sea conditions can lead to improved safety for ships and better weather predictions.
Who this helps: This helps ship operators and meteorologists.
Reorganization of the endoscopic activity of Cancer Institutes during phase II of the Covid-19 emergency.
2020
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
Fiori G, Trovato C, Staiano T, Magarotto A, Stigliano V +7 more
Plain English This research studied how cancer treatment centers reorganized their endoscopic procedures during the COVID-19 pandemic's second phase. It found that due to safety concerns, many endoscopic procedures were reduced, requiring doctors to prioritize patients at higher risk for digestive tumors, which led to longer wait times for some. This matters because ensuring that cancer patients receive timely care while minimizing COVID-19 risks is crucial for their health outcomes.
Who this helps: This helps cancer patients who need endoscopic procedures and their doctors managing treatment plans.
Design and Synthesis of Chitosan-Gelatin Hybrid Hydrogels for 3D PrintableModels.
2020
Frontiers in chemistry
Magli S, Rossi GB, Risi G, Bertini S, Cosentino C +7 more
Plain English This study focused on creating new materials called hybrid hydrogels made from chitosan and gelatin that can be used for 3D printing. Researchers found that these hydrogels have special properties that allow them to be shaped easily and are safe for living cells. This is important because it could lead to better tools for medical applications, like creating tissue structures or drug delivery systems.
Who this helps: This benefits patients needing advanced medical treatments and doctors using new 3D printing technologies.
A Negative Allosteric Modulator of WNT Receptor Frizzled 4 Switches into an Allosteric Agonist.
2018
Biochemistry
Riccio G, Bottone S, La Regina G, Badolati N, Passacantilli S +6 more
Plain English This study looked at a new molecule called FzM1.8, which affects a receptor involved in cell signaling known as Frizzled 4. Researchers found that FzM1.8 activates this receptor, encouraging certain cancer cells, specifically colon cancer cells, to grow and maintain their undifferentiated state. This matters because it could help scientists understand how to target WNT signaling in cancer treatment.
Who this helps: This helps researchers and doctors working on colon cancer therapies.
Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients.
2018
Cancer genetics
Liccardo R, De Rosa M, Rossi GB, Rigler G, Izzo P +1 more
Plain English This study focused on identifying large changes in the MSH2 gene linked to Lynch syndrome, a genetic condition that increases cancer risk. Researchers found a significant duplication in the MSH2 gene in three unrelated patients, specifically a region that is 14,846 base pairs long, indicating a possible common origin for this genetic change. Understanding these large duplications helps improve genetic testing and counseling for Lynch syndrome, potentially allowing for earlier cancer detection and prevention.
Who this helps: This helps patients with Lynch syndrome and their families by providing insights for better genetic testing and risk management.
Large polypoid perineurioma of the transverse colon without crypt serration (NPS).
2018
International journal of clinical and experimental pathology
Cantile M, Cerrone M, Amore A, Rossi GB, Tatangelo F +2 more
Plain English This study looked at a specific type of growth called intestinal perineurioma found in the transverse colon. Researchers found that this growth was much larger than usual, measuring about 4.5 cm, while typical sizes range from 0.2 to 0.6 cm. Understanding these differences is important because it helps doctors recognize and differentiate these tumors from other types of growths, improving diagnosis and treatment.
Who this helps: Patients who have or are at risk for intestinal tumors.
Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.
2017
International journal of molecular sciences
Liccardo R, De Rosa M, Rossi GB, Carlomagno N, Izzo P +1 more
Plain English This study focused on finding genetic mutations in people who may have Lynch syndrome, a hereditary form of colorectal cancer. Researchers examined 97 individuals and found 27 genetic variants, including nine that were previously unknown. They determined that three of these new variants were harmful and linked to the disease, while other variants didn’t show a clear connection to Lynch syndrome in some family cases, suggesting that other genetic factors may also play a role.
Who this helps: This helps patients and families affected by Lynch syndrome understand the complexities of their genetic risks.
Comparison of Grain Proteome Profiles of Four Brazilian Common Bean (Phaseolus vulgaris L.) Cultivars.
2017
Journal of agricultural and food chemistry
Rossi GB, Valentim-Neto PA, Blank M, Faria JC, Arisi ACM
Plain English Researchers studied four types of common beans grown in Brazil to compare their protein content. They found 32 different proteins that varied among the bean types, particularly noting that storage proteins like phaseolins and legumins were the most common. This is important because understanding the protein profiles can help improve bean quality and yields for farmers and benefit consumers.
Who this helps: This research helps farmers and consumers of common beans.
WNT Inhibitory Activity of Malus Pumila miller cv Annurca and Malus domestica cv Limoncella Apple Extracts on Human Colon-Rectal Cells Carrying Familial Adenomatous Polyposis Mutations.
2017
Nutrients
Riccio G, Maisto M, Bottone S, Badolati N, Rossi GB +3 more
Plain English This study looked at how extracts from two types of Italian apples, Annurca and Limoncella, can block a specific pathway that leads to the growth of cancer cells in people with Familial Adenomatous Polyposis (FAP). The apple extracts were found to be effective inhibitors of this pathway, with concentrations that could be relevant for consumers. However, the beneficial effects were reduced during digestion, suggesting that a special coating is needed to ensure the extracts work properly in the digestive system.
Who this helps: This research could benefit patients with Familial Adenomatous Polyposis and their treatment options.
Leaf proteome comparison of two GM common bean varieties and their non-GM counterparts by principal component analysis.
2016
Journal of the science of food and agriculture
Valentim-Neto PA, Rossi GB, Anacleto KB, de Mello CS, Balsamo GM +1 more
Plain English This study compared the protein profiles of two genetically modified (GM) common bean varieties and their non-GM counterparts to see how they differed. Researchers found that while there were some noticeable differences in the proteins when comparing GM beans to non-GM beans, the GM variety was actually more similar to its non-GM version than it was to other non-GM varieties. This is important because it helps us understand how GM crops can be similar to traditional crops in terms of their biological makeup.
Who this helps: This benefits farmers and consumers who want to know more about the similarities and differences between GM and non-GM crops.
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures.
2015
International journal of oncology
Costabile V, Duraturo F, Delrio P, Rega D, Pace U +6 more
Plain English This study looked at how lithium chloride (LiCl) can affect colon cancer cells in the lab. Researchers found that when they treated these cells with LiCl for 10 days, the cells started to regain some characteristics of normal epithelial cells, indicated by increased levels of E-cadherin, while markers associated with a cancerous, more mobile state decreased. This is important because it suggests that LiCl could be a potential treatment to help reverse aggressive cancer traits in patients with colon cancer.
Who this helps: This research benefits patients with colon cancer by exploring new treatment options.
Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability.
2015
International journal of molecular medicine
Duraturo F, Liccardo R, Cavallo A, De Rosa M, Rossi GB +1 more
Plain English This study looked at the role of certain genetic mutations in patients with colorectal cancer who have a condition called microsatellite instability (MSI). Researchers found that 73% of patients with high MSI levels had harmful mutations in the MLH1 and MSH2 genes, compared to only 9% of those with low MSI. They also discovered two new mutations in the MLH1 gene that could contribute to cancer, underscoring the importance of genetic testing for patients at risk of hereditary colorectal cancer.
Who this helps: This research benefits patients at risk for hereditary colorectal cancer and their healthcare providers.
Role of endoscopic ultrasonography in the loco-regional staging of patients with rectal cancer.
2015
World journal of gastrointestinal endoscopy
Marone P, de Bellis M, D'Angelo V, Delrio P, Passananti V +5 more
Plain English In this study, researchers looked at how effective endoscopic ultrasonography (EUS) is for staging rectal cancer, which is important for determining the best treatment options. They found that EUS is very accurate, especially for determining the extent of the tumor in early-stage rectal cancer, but it is less reliable for assessing cancer after treatment before surgery. This matters because having the right information about the cancer stage helps doctors decide on the most effective treatment for patients, improving outcomes.
Who this helps: Patients with rectal cancer and their doctors.
A specific endogenous reference for genetically modified common bean (Phaseolus vulgaris L.) DNA quantification by real-time PCR targeting lectin gene.
2014
Molecular biotechnology
Venturelli GL, Brod FC, Rossi GB, Zimmermann NF, Oliveira JP +2 more
Plain English This study focused on creating a reliable method to measure genetically modified (GM) common beans using a specific DNA test. Researchers found that the method using the lectin gene was highly effective, accurately detecting both GM and non-GM beans with a detection limit as low as ten copies of the bean’s DNA. This is important because it allows for clear tracking and regulation of GM beans in the market, ensuring consumer safety and adherence to agricultural standards.
Who this helps: This helps farmers, food safety regulators, and consumers.
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome.
2013
Hereditary cancer in clinical practice
Paparo L, Rossi GB, Delrio P, Rega D, Duraturo F +4 more
Plain English This study looked at three families with genetic mutations in the PTEN gene, which is linked to conditions known as PTEN hamartoma tumor syndrome. The researchers found that different mutations led to very different health issues among family members, including a unique mutation not seen before in one family. Notably, one elderly patient had very low PTEN levels, which were linked to a rare set of health problems and cancer. This matters because it helps us understand why people in the same family with the same gene mutation can experience such different symptoms and risks.
Who this helps: Patients and families affected by PTEN hamartoma tumor syndrome.
Synergistic effect of interleukin-10-receptor variants in a case of early-onset ulcerative colitis.
2013
World journal of gastroenterology
Galatola M, Miele E, Strisciuglio C, Paparo L, Rega D +7 more
Plain English This study focused on understanding the genetic causes of early-onset ulcerative colitis (UC) in an 18-month-old child. Researchers found that the child had specific genetic changes in the IL10 receptor genes, which likely contributed to the disease. They discovered that both the child’s relatives and the child showed abnormal protein levels in their blood related to inflammation, indicating that these changes might be markers for the disease in family members.
Who this helps: This research benefits families with early-onset ulcerative colitis by providing insights into genetic risk factors.
Beta catenin and cytokine pathway dysregulation in patients with manifestations of the "PTEN hamartoma tumor syndrome".
2012
BMC medical genetics
Galatola M, Paparo L, Duraturo F, Turano M, Rossi GB +2 more
Plain English This study examined patients with a genetic condition called PTEN hamartoma tumor syndrome (PHTS), which increases the risk of various cancers. Researchers found that blood cells from these patients had higher levels of a protein called beta-catenin and changes in important signaling molecules associated with inflammation, specifically TNF-alpha and its receptors. These findings are important because they reveal a potential link between the genetic mutation affecting PTEN and the increased cancer risk by affecting cell survival and inflammation in the body.
Who this helps: This information benefits patients with PHTS and their doctors by improving understanding of the condition's mechanisms and cancer risk.
Is flexible bronchoscopy necessary to confirm the position of double-lumen tubes before thoracic surgery?
2011
European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery
de Bellis M, Accardo R, Di Maio M, La Manna C, Rossi GB +3 more
Plain English This study looked at whether it's really necessary to use a flexible bronchoscope to check the placement of double-lumen tubes in patients before thoracic surgery. They found that 37% of the tubes were not in the right position initially, even though the anesthesiologist thought they were, and 5% of patients had critically misplaced tubes that needed immediate adjustment. This is important because it highlights that checking with a bronchoscope can help avoid complications during surgery.
Who this helps: This helps doctors and patients undergoing thoracic surgery.
Endoscopic palliation in patients with incurable malignant colorectal obstruction by means of self-expanding metal stent: analysis of results and predictors of outcomes in a large multicenter series.
2011
Archives of surgery (Chicago, Ill. : 1960)
Manes G, de Bellis M, Fuccio L, Repici A, Masci E +6 more
Plain English This study looked at how well self-expanding metal stents (SEMS) work for patients with incurable colorectal cancer who experience blockage in their intestines. Out of 201 patients, 91.5% had successful placement of the stent, and 89.7% of those saw improvement in their bowel function, resulting in normal bowel movements for an average of about 115 days. Overall, this method allows about 75% of patients to avoid needing a colostomy, which is important for maintaining a better quality of life.
Who this helps: This helps patients with incurable colorectal cancer who face bowel obstruction.
Endoscopic surveillance for hereditary non-polyposis colorectal cancer (HNPCC) family members in a Southern Italian region.
2010
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
Esposito I, de Bellis M, de Leone A, Rossi GB, Selvaggi F +7 more
Plain English This study looked at how well family members of people with hereditary non-polyposis colorectal cancer (HNPCC) followed guidelines for routine colon checks. Researchers reviewed data from 106 family members, finding that 40 participated in surveillance, and during their first check-ups, they discovered 7 cases of colorectal cancer and 14 polyps. The results showed that regular colonoscopies every two years are effective for catching serious problems early and help family members stick to their health guidelines.
Who this helps: This helps family members of HNPCC patients by monitoring their health more effectively.
Ponti G, Losi L, Pellacani G, Rossi GB, Presutti L +8 more
Plain English This study looked at a rare tumor called juvenile nasopharyngeal angiofibroma (JNA) and its association with familial adenomatous polyposis (FAP), a genetic condition. Researchers examined tissue samples from patients who had JNA surgery between 1991 and 2006 and found that 25% of young patients also had FAP linked to a specific genetic mutation. The study revealed that both types of JNA showed similar biological markers, suggesting that testing for these markers could help identify patients at risk for FAP and that new treatments targeting specific pathways might improve therapy for these tumors.
Who this helps: This helps patients diagnosed with juvenile nasopharyngeal angiofibroma, particularly those at risk for familial adenomatous polyposis.
Alternative splicing and nonsense-mediated mRNA decay in the regulation of a new adenomatous polyposis coli transcript.
2007
Gene
De Rosa M, Morelli G, Cesaro E, Duraturo F, Turano M +3 more
Plain English This study investigated a gene called "apc," which is linked to a hereditary condition called familial adenomatous polyposis (FAP) that can lead to cancer. Researchers identified nine new variants of the apc transcript, with three of them producing important proteins needed for regulating cell growth and development, while six others created faulty versions that the cell normally breaks down. They found that the presence of one of these faulty variants changes during the development of colorectal cancer, suggesting that the regulation of these transcripts is important for understanding how FAP contributes to cancer risk.
Who this helps: This research benefits patients with familial adenomatous polyposis and their doctors by providing insights into how the disease affects cancer risk.
Identification and classification of hereditary nonpolyposis colorectal cancer (Lynch syndrome): adapting old concepts to recent advancements. Report from the Italian Association for the study of Hereditary Colorectal Tumors Consensus Group.
2007
Diseases of the colon and rectum
Ponz de Leon M, Bertario L, Genuardi M, Lanza G, Oliani C +5 more
Plain English This study looked at how to identify and classify Lynch syndrome, a hereditary form of colorectal cancer, based on the latest research. The authors recommend keeping the term "Lynch syndrome" for families with specific DNA repair issues and using "clinical hereditary nonpolyposis colorectal cancer" for others who meet certain criteria but don't have those issues. They also emphasize the importance of regular check-ups for high-risk family members, starting at age 20-25, while newer testing methods are becoming available in labs.
Who this helps: This helps patients and families at risk for Lynch syndrome and doctors who treat them.
[Early evaluation using PET-FDG of the efficiency of neoadjuvant radiochemotherapy treatment in locally advanced neoplasia of the lower rectum].
2003
Tumori
Delrio P, Lastoria S, Avallone A, Ravo V, Guida C +19 more
Plain English Researchers studied how well a special imaging method called PET-FDG can assess the effectiveness of pre-surgery treatment for patients with advanced rectal cancer. They found that this imaging technique was able to show whether the tumor was shrinking as early as 10 to 15 days after starting treatment, helping to identify patients who were not responding well. This is important because it allows doctors to adjust treatment plans sooner, potentially improving outcomes for patients.
Who this helps: This benefits patients with advanced rectal cancer and their doctors.
The mutation spectrum of the APC gene in FAP patients from southern Italy: detection of known and four novel mutations.
2003
Human mutation
De Rosa M, Scarano MI, Panariello L, Morelli G, Riegler G +6 more
Plain English This study examined the APC gene, which is linked to familial adenomatous polyposis (FAP), a genetic condition that can lead to colorectal cancer. Researchers looked at 40 families with FAP and found 30 mutations in the APC gene, including 22 different types, four of which had never been seen before. Understanding these mutations is important because it helps predict the severity of FAP and improve genetic testing, which can lead to earlier interventions and better patient outcomes.
Who this helps: This benefits patients with FAP and their families by providing more information for better management of the disease.
Daniele B, Rossi GB, Losito S, Gridelli C, de Bellis M
Plain English This study looked at a 49-year-old woman with cancer who experienced mild ischemic colitis after receiving chemotherapy that included the drug paclitaxel. She had symptoms like abdominal pain and bloody diarrhea, which went away in about 10 days. The findings highlight that ischemic colitis can happen in cancer patients on paclitaxel, especially when they have normal white blood cell counts, which is important for doctors to consider when diagnosing gastrointestinal issues after chemotherapy.
Who this helps: This helps patients undergoing chemotherapy and their doctors in identifying complications related to treatment.
Phenotype-genotype correlations in an extended family with adenomatosis coli and an unusual APC gene mutation.
2001
Diseases of the colon and rectum
Ponz de Leon M, Varesco L, Benatti P, Sassatelli R, Izzo P +7 more
Plain English This study looked at a family in southern Italy affected by familial adenomatous polyposis (FAP), a genetic condition that can cause numerous polyps in the intestines and other severe complications, including desmoid tumors. They found that 15 family members had FAP, and 11 of those (about 73%) developed desmoid tumors, which were particularly severe for four of them, leading to two deaths related to these tumors. The researchers discovered a unique mutation in the APC gene responsible for this condition, which may help explain why certain mutations are linked to a higher risk of developing desmoid tumors.
Who this helps: This information is beneficial for patients with familial adenomatous polyposis and their doctors, improving understanding and management of related health risks.
Granular cell tumors of the colon: report of a case and review of the literature.
2000
Journal of clinical gastroenterology
Rossi GB, de Bellis M, Marone P, De Chiara A, Losito S +1 more
Plain English This study looked at a rare type of tumor called granular cell tumors in the colon, focusing on a 38-year-old man who was found to have multiple tumors during a screening colonoscopy. Out of 55 reported cases in the literature, only 15 involved multiple tumors; however, there is no evidence to connect these tumors with colorectal cancer. Since these tumors are usually non-cancerous, the authors recommend careful monitoring and, if needed, removing the tumors using a minimally invasive procedure.
Who this helps: This information benefits patients with similar tumors and their doctors.
Expression of cripto and amphiregulin in colon mucosa from high risk colon cancer families.
1999
International journal of oncology
De Angelis E, Grassi M, Gullick WJ, Johnson GR, Rossi GB +5 more
Plain English This study examined two specific proteins, cripto-I and amphiregulin, in the colon tissue of people at high risk for colon cancer. The researchers found that cripto-I was present in 62% of colon samples from high-risk individuals and only in 20% from those at normal risk, while amphiregulin was found in 69% of high-risk samples versus 80% in low-risk samples. These findings suggest that high levels of cripto-I and changes in amphiregulin expression may be early signs of colon cancer development, which could help identify people at greater risk.
Who this helps: This helps patients who are at high risk for colon cancer.
Familial adenomatous polyposis coli: five novel mutations in exon 15 of the adenomatous polyposis coli (APC) gene in Italian patients. Mutations in brief no. 225. Online.
1999
Human mutation
Scarano MI, De Rosa M, Panariello L, Carlomagno N, Riegler G +6 more
Plain English This study looked at mutations in a gene called APC that are linked to a hereditary condition known as familial adenomatous polyposis (FAP), which increases the risk of colorectal cancer. The researchers discovered five new mutations in a specific part of the APC gene, with one patient showing severe symptoms starting at age 12 and another showing a milder form of the disease. This research highlights how different mutations can lead to very different health outcomes for patients.
Who this helps: This benefits patients with familial adenomatous polyposis and their doctors.
Mucosal expression of carcinoembryonic antigen and carbohydrate antigen 19-9 in patients with gastritis and gastric cancer.
1999
Cancer detection and prevention
Esposito G, Tempesta A, Galati MG, de Bellis M, Rossi GB +4 more
Plain English This study looked at 68 patients to see how useful certain proteins (CEA and CA19-9) in stomach tissue could be for spotting people at high risk for gastric cancer. The researchers found that the levels of these proteins increased significantly from those with mild gastritis to those with atrophic gastritis and gastric cancer, with specific increases in CA19-9 and CEA levels (p = 0.005 and p = 0.002). This is important because it could help identify patients who need closer monitoring for gastric cancer risk based on these protein levels.
Who this helps: This research benefits patients at risk for gastric cancer and their doctors by improving early detection strategies.
Prevalence of HNPCC in a series of consecutive patients on the first endoscopic diagnosis of colorectal cancer: a multicenter study. The Italian Collaborative Group.
1999
Endoscopy
Riegler G, Savastano A, Selvaggi F, Ciociano R, Martino R +20 more
Plain English This study looked at how common hereditary non-polyposis colorectal cancer (HNPCC) is among patients diagnosed with colorectal cancer in Italy. They assessed family histories for 485 patients and found that only 1% met the strict criteria for HNPCC, but if they relaxed the criteria slightly, that number increased to 3%. This is important because it helps identify families at risk, making it easier to spot genetic mutations and provide preventive care for healthy relatives.
Who this helps: This helps patients and their families by improving early detection and prevention strategies.
Three submicroscopic deletions at the APC locus and their rapid detection by quantitative-PCR analysis.
1999
European journal of human genetics : EJHG
De Rosa M, Scarano MI, Panariello L, Carlomagno N, Rossi GB +4 more
Plain English This study looked at three families with a genetic condition called familial adenomatous polyposis (FAP), which leads to the development of multiple polyps in the colon and increased cancer risk. Researchers found that these families had small missing pieces of DNA at a specific site in their genes, including the APC gene, which is crucial for preventing colon cancer. By using a special genetic testing technique, they were able to quickly identify these deletions, which is important because it helps diagnose FAP in patients when standard tests do not find any mutations.
Who this helps: This research benefits patients with familial adenomatous polyposis and their families by providing better diagnostic options.
hMLH1 mutations in hereditary nonpolyposis colorectal cancer kindreds. Mutations in brief no. 182. Online.
1998
Human mutation
Panariello L, Scarano MI, de Rosa M, Capasso L, Renda A +4 more
Plain English This study focused on hereditary nonpolyposis colorectal cancer (HNPCC), which is a genetic condition that increases the risk of early colorectal cancer. Researchers analyzed 10 Italian families and discovered three new changes (mutations) in the hMLH1 gene, which is important for DNA repair. One of these mutations, a deletion causing an early stop in protein production, is likely to disrupt normal protein function, while the other two mutations significantly alter crucial regions of the hMLH1 protein.
Who this helps: This research helps patients with a family history of HNPCC by improving genetic understanding and screening for potential cancer risks.
Is transcranial Doppler effective in avoiding the hazards of carotid surgery?
1996
Cardiovascular surgery (London, England)
Bornstein NM, Rossi GB, Treves TA, Shifrin EG
Plain English This study looked at whether a method called transcranial Doppler, which measures blood flow in the brain, is useful for monitoring patients during carotid surgery. Researchers found that when the blood flow was temporarily blocked during the procedure, the speed of blood flow decreased significantly from 97 to 45 cm/s. Although eight patients showed some neurological symptoms during the surgery and three had minor strokes afterwards, the blood flow changes were similar in patients with and without complications, indicating that this monitoring technique may not be helpful in deciding if a safety device should be used during surgery.
Who this helps: This information is particularly relevant for doctors and surgical teams performing carotid surgeries.
Interferon alpha-2b and retinoic acid combined treatment affects proliferation and gene expression of human cervical carcinoma cells.
1995
Cancer research
Lancillotti F, Giandomenico V, Affabris E, Fiorucci G, Romeo G +1 more
Plain English This study looked at how combining two treatments, interferon alpha-2b and retinoic acid, affects the growth of cervical cancer cells in a lab setting. The researchers found that this combination slows down cell growth more effectively than either treatment alone, increasing the activity of specific genes that help fight cancer. Specifically, the combination boosted the levels of a gene important in cancer response and also increased another gene linked to immune response.
Who this helps: This helps patients with cervical cancer by potentially providing a more effective treatment option.