Anne R Diers

Candel Therapeutics, Inc., Needham, Massachusetts.

27 publications 2009 – 2025 ORCID

What does Anne R Diers research?

Dr. Diers investigates how different therapies, particularly those targeting cancer cell metabolism and immune modulation, can lead to improved treatment options for various types of cancer, including pancreatic cancer, glioblastoma, and prostate cancer. For example, she studies innovative virus-based treatments and compounds that exploit the vulnerabilities of cancer cells, looking at their effects on tumor growth and immune cell activation. Additionally, her research explores the biochemical pathways involved in cell division and how stress affects normal and cancerous cells, providing insights essential for developing safer, more effective cancer therapies.

Key findings

  • CAN-2409 treatment stopped tumor growth and boosted CD8+ T cell activity in mice, suggesting improved cancer therapies.
  • BPM31510, a treatment delivering ubidecarenone, significantly increased long-term survival rates by over 25% in animal models of glioblastoma.
  • Oxidized Coenzyme Q treatment induced cell death in pancreatic cancer cells and organoids, representing a novel therapeutic approach.
  • Proteins Filamin-A and Filamin-B were identified as differentially expressed in prostate cancer patients, which may serve as new biomarkers for diagnosis.
  • KISS1 protein increased mitochondrial numbers by 30% to 50% in cancer cells, potentially preventing metastasis.

Frequently asked questions

Does Dr. Diers study pancreatic cancer?
Yes, Dr. Diers conducts research on pancreatic cancer, focusing on novel treatments that target the disease's unique cellular metabolism.
What treatments has Dr. Diers researched?
She has researched several treatments, including a virus-based therapy called CAN-2409 and the compound BPM31510, which targets cancer cell metabolism.
Is Dr. Diers's work relevant to patients with aggressive cancers?
Absolutely. Her studies are particularly relevant for patients with aggressive cancers like pancreatic cancer and glioblastoma, offering new treatment options.
Can Dr. Diers's research help improve cancer diagnosis?
Yes, her identification of potential biomarkers for various cancers, such as Filamin-A and Filamin-B in prostate cancer, aims to enhance diagnostic accuracy.
What impact does Dr. Diers's work have on cancer treatments?
Her work aims to provide safer and more effective treatment options by understanding cancer cell vulnerabilities and immune responses, ultimately improving patient outcomes.

Publications in plain English

Dynamic Tracking of Tumor Microenvironment Modulation Using Kaede Photoconvertible Transgenic Mice Unveils New Biological Properties of Viral Immunotherapy.

2025

Cancer research communications

Diers AR, Guo Q, Li Z, Richardson E, Idris S +4 more

Plain English
This study looked at how a new virus-based treatment called CAN-2409 affects tumors and the immune response in mice. The researchers found that this treatment not only stopped tumor growth but also significantly boosted the activity of certain immune cells known as CD8+ T cells, which are important for fighting cancer. Specifically, new and existing CD8+ T cells in the tumor became more active and proliferative after the treatment. These findings are important because they suggest that combining CAN-2409 with another treatment could lead to better outcomes for cancer patients. Who this helps: This helps cancer patients by improving potential treatment options.

PubMed

Elevated levels of mitochondrial CoQinduce ROS-mediated apoptosis in pancreatic cancer.

2021

Scientific reports

Dadali T, Diers AR, Kazerounian S, Muthuswamy SK, Awate P +22 more

Plain English
This study focused on using a compound called oxidized Coenzyme Q to see how it affects pancreatic cancer cells. The researchers found that applying this compound increased levels of reactive oxygen species (ROS), which led to cell death in pancreatic cancer cells, as well as in organoids from human patients and tumor models. This is significant because it shows a new way to potentially treat pancreatic cancer by targeting mitochondrial function, highlighting a treatment called BPM31510 that could benefit patients with cancers that generate a lot of ROS. Who this helps: Patients with pancreatic cancer and potentially other cancers that are sensitive to this treatment.

PubMed

Ubc1 turnover contributes to the spindle assembly checkpoint in Saccharomyces cerevisiae.

2021

G3 (Bethesda, Md.)

Arsenault HE, Ghizzoni JM, Leech CM, Diers AR, Gesta S +4 more

Plain English
This study examined how a protein called Ubc1 affects the spindle assembly checkpoint in yeast cells. Researchers discovered that increasing Ubc1 levels helped yeast survive treatments that disrupt cell division, while reducing Ubc1 made them more vulnerable. The findings highlight the important role of Ubc1 in managing how cells respond to signals that ensure chromosomes are properly divided, which is crucial for maintaining genetic stability. Who this helps: This helps researchers studying cell division and genetic stability.

PubMed

High levels of ubidecarenone (oxidized CoQ) delivered using a drug-lipid conjugate nanodispersion (BPM31510) differentially affect redox status and growth in malignant glioma versus non-tumor cells.

2020

Scientific reports

Sun J, Patel CB, Jang T, Merchant M, Chen C +9 more

Plain English
This study looked at a treatment called BPM31510, which delivers high levels of ubidecarenone (a form of Coenzyme Q) specifically to cancer cells in order to exploit their vulnerabilities. The researchers found that cancer cells, like glioblastoma, were much more sensitive to this treatment compared to non-cancer cells, resulting in a significant increase in cell death and a greater than 25% long-term survival rate in animal models. This matters because it could lead to more effective therapies for aggressive brain tumors, which are often resistant to standard treatments. Who this helps: This helps patients with glioblastoma and their doctors by providing new potential treatment options.

PubMed

Thiolate-based dinitrosyl iron complexes: Decomposition and detection and differentiation from S-nitrosothiols.

2017

Nitric oxide : biology and chemistry

Keszler A, Diers AR, Ding Z, Hogg N

Plain English
This study focused on a specific type of iron complex called dinitrosyl iron complexes (DNIC), which are formed in solutions with iron and nitric oxide. Researchers found that these complexes remain stable for hours under neutral conditions but break down when other compounds (thiols) are present, producing nitrite instead. This is important because it means that previous measurements of S-nitrosothiols (another type of compound) could be inaccurate if mercury chloride was used in the testing process. Who this helps: This benefits scientists and researchers working on nitric oxide-related studies in cells.

PubMed

Identification of Filamin-A and -B as potential biomarkers for prostate cancer.

2017

Future science OA

Narain NR, Diers AR, Lee A, Lao S, Chan JY +17 more

Plain English
Researchers studied two proteins, Filamin-A (FLNA) and Filamin-B (FLNB), to see if they could be used as indicators for prostate cancer. They found that FLNA and FLNB appeared differently in patients with prostate cancer compared to those without; specifically, in healthy individuals, their blood levels were linked, while this connection was disrupted in cancer patients. Finding reliable markers for prostate cancer is important because it can lead to better diagnosis and treatment. Who this helps: This helps patients with prostate cancer and their doctors.

PubMed

Cancer cell metabolism and the modulating effects of nitric oxide.

2015

Free radical biology & medicine

Chang CF, Diers AR, Hogg N

Plain English
This study looked at how cancer cells change their energy use and how nitric oxide (NO) plays a role in this process. Researchers found that a protein called NOS2, which produces NO, is associated with more aggressive types of cancer, like melanoma and breast cancer. Understanding this relationship is important because it could lead to new ways to target and treat aggressive tumors. Who this helps: This helps patients with aggressive cancers and their doctors by informing treatment strategies.

PubMed

A novel class of mitochondria-targeted soft electrophiles modifies mitochondrial proteins and inhibits mitochondrial metabolism in breast cancer cells through redox mechanisms.

2015

PloS one

Vayalil PK, Oh JY, Zhou F, Diers AR, Smith MR +6 more

Plain English
Researchers studied a new type of treatment designed to target the energy-producing parts of breast cancer cells, known as mitochondria. They found that a specific compound, called IBTP, significantly reduced the growth and movement of these cancer cells by disrupting their energy production, leading to less cell attachment and proliferation. This finding matters because it could lead to new, less toxic therapies that specifically attack cancer cells after conventional treatments fail. Who this helps: This helps breast cancer patients looking for more effective treatment options.

PubMed

Inhibition of an NAD⁺ salvage pathway provides efficient and selective toxicity to human pluripotent stem cells.

2015

Stem cells translational medicine

Kropp EM, Oleson BJ, Broniowska KA, Bhattacharya S, Chadwick AC +7 more

Plain English
Researchers found that a drug called STF-31 can kill undifferentiated stem cells while leaving normal cells alone, by blocking a specific pathway cells use to recycle a molecule called NAD⁺. This matters because stem cell therapies have a cancer risk—if any undifferentiated stem cells slip into a treatment, they could form tumors—so a way to reliably eliminate them before use makes these therapies much safer to use in patients.

PubMed

Detection of S-nitrosothiols.

2014

Biochimica et biophysica acta

Diers AR, Keszler A, Hogg N

Plain English
This research paper focuses on how to accurately detect and analyze S-nitrosothiols, which are important compounds related to nitric oxide in the body. The authors highlight various methods for detection, noting that each has its own strengths and weaknesses. They emphasize the need for reliable techniques to avoid misleading results, as mistakes in measurement can easily occur. Who this helps: This benefits researchers and healthcare professionals who study or work with nitric oxide and its effects in the body.

PubMed

Metastasis suppressor KISS1 seems to reverse the Warburg effect by enhancing mitochondrial biogenesis.

2014

Cancer research

Liu W, Beck BH, Vaidya KS, Nash KT, Feeley KP +8 more

Plain English
This research looked at how a protein called KISS1 affects cancer cell behavior, particularly how cancer cells use energy. It was found that KISS1 reduces a method cancer cells use to metabolize glucose (called the Warburg effect), leading to a healthier way of producing energy through mitochondria. Specifically, cells with KISS1 had 30% to 50% more mitochondria than those lacking it, which is important because it may help prevent the spread of cancer. Who this helps: This benefits cancer patients and doctors by providing insights into potential new treatments to stop metastasis.

PubMed

S-Nitrosation of monocarboxylate transporter 1: inhibition of pyruvate-fueled respiration and proliferation of breast cancer cells.

2014

Free radical biology & medicine

Diers AR, Broniowska KA, Chang CF, Hill RB, Hogg N

Plain English
Researchers studied how a chemical process called S-nitrosation affects the energy production and growth of breast cancer cells. They found that this process reduced the cells' ability to take in a key energy source called pyruvate and significantly hindered their growth, with both types of S-nitrosating agents used leading to reduced cell growth. This research reveals that targeting the energy metabolism of cancer cells could be a new way to limit their growth. Who this helps: This helps patients with breast cancer and doctors seeking new treatment strategies.

PubMed

S-nitrosoglutathione.

2013

Biochimica et biophysica acta

Broniowska KA, Diers AR, Hogg N

Plain English
This study examines S-nitrosoglutathione (GSNO), a compound derived from glutathione, which plays a key role in how nitric oxide affects cells and has links to various diseases. Researchers found that GSNO works in several ways to influence cellular actions, making it a significant point of interest for potential treatments. Understanding GSNO is important because it could lead to new therapies for diseases where nitric oxide signaling is disrupted. Who this helps: This helps patients dealing with diseases affected by nitric oxide signaling.

PubMed

Effect of nitric oxide on naphthoquinone toxicity in endothelial cells: role of bioenergetic dysfunction and poly (ADP-ribose) polymerase activation.

2013

Biochemistry

Broniowska KA, Diers AR, Corbett JA, Hogg N

Plain English
This study examined how nitric oxide (NO) and a toxic compound called naphthoquinone affect the health of cells that line blood vessels (endothelial cells). Researchers found that when these cells are exposed to both NO and reactive oxygen species (ROS), their energy-producing structures (mitochondria) suffer damage, leading to a significant loss of energy molecules and ultimately causing cell death. Specifically, the presence of both NO and ROS led to mitochondrial dysfunction, affecting energy metabolism and cell survival, but inhibiting a specific cell death pathway (PARP) did not improve cell viability. Who this helps: This research benefits patients with conditions affecting blood vessels, such as cardiovascular diseases, by providing insights into the mechanisms of cell damage.

PubMed

Mitochondrial bioenergetics of metastatic breast cancer cells in response to dynamic changes in oxygen tension: effects of HIF-1α.

2013

PloS one

Diers AR, Vayalil PK, Oliva CR, Griguer CE, Darley-Usmar V +3 more

Plain English
This study looked at how breast cancer cells adapt to low oxygen levels, which are common in tumors. Researchers found that metastatic breast cancer cells were able to adjust their energy production and become more efficient as oxygen decreased, while non-cancerous cells did not respond in the same way. Specifically, the malignant cells increased their use of glucose and maintained higher energy production even in extreme low oxygen conditions, which helps them survive and spread. Who this helps: This research benefits patients with metastatic breast cancer by paving the way for new treatments that target their energy production mechanisms.

PubMed

Nitrosative stress and redox-cycling agents synergize to cause mitochondrial dysfunction and cell death in endothelial cells.

2013

Redox biology

Diers AR, Broniowska KA, Hogg N

Plain English
This study looked at how two types of stress—nitrosative stress from a compound called S-nitrosocysteine and redox-cycling agents that produce damaging molecules—affect cells that line blood vessels. The researchers found that while S-nitrosocysteine alone disrupts the energy production in these cells, it doesn’t cause them to die by itself. However, when combined with redox-cycling agents, it leads to more energy depletion and cell death, indicating that this combination is particularly harmful to endothelial cells. Who this helps: This research benefits doctors and patients by improving our understanding of conditions like heart disease, where blood vessel function is compromised.

PubMed

Subsets of ATP-sensitive potassium channel (KATP) inhibitors increase gap junctional intercellular communication in metastatic cancer cell lines independent of SUR expression.

2012

FEBS letters

Bodenstine TM, Vaidya KS, Ismail A, Beck BH, Diers AR +4 more

Plain English
The study looked at how certain inhibitors of ATP-sensitive potassium channels (KATP) can improve communication between cancer cells. Researchers found that using these inhibitors increased the rate of communication between metastatic cancer cells by 50% on average, regardless of the level of specific proteins (SUR1 and SUR2) in those cells. This matters because improving cell communication could slow down the progression of cancer. Who this helps: This research helps cancer patients by providing insights that could lead to better treatment options.

PubMed

Cell signalling by reactive lipid species: new concepts and molecular mechanisms.

2012

The Biochemical journal

Higdon A, Diers AR, Oh JY, Landar A, Darley-Usmar VM

Plain English
This study looked at how certain fatty molecules, called reactive lipid species (RLS), communicate within cells. Researchers found that these molecules can change specific proteins by attaching to them, which helps with important processes like reducing inflammation, managing cell death, and boosting cellular defenses against damage. The study highlights that this kind of communication can create lasting signals in cells, which is important for maintaining health and responses to stress. Who this helps: This benefits patients undergoing treatments for inflammation or conditions related to cell dysfunction.

PubMed

Pyruvate fuels mitochondrial respiration and proliferation of breast cancer cells: effect of monocarboxylate transporter inhibition.

2012

The Biochemical journal

Diers AR, Broniowska KA, Chang CF, Hogg N

Plain English
This study looked at how breast cancer cells use pyruvate, a substance produced during glucose metabolism, to grow and thrive. The researchers found that when breast cancer cells were given more pyruvate, their growth increased significantly compared to when they had lactate, with pyruvate bolstering their energy production in mitochondria. Additionally, blocking the intake of pyruvate into cells slowed down their growth and energy usage, showing that targeting this process could be a new way to fight breast cancer. Who this helps: This research benefits patients with breast cancer by suggesting new treatment strategies.

PubMed

Oxidative modification of proteins: an emerging mechanism of cell signaling.

2012

Frontiers in physiology

Wall SB, Oh JY, Diers AR, Landar A

Plain English
This study looks at how certain reactive molecules in the body can modify proteins, a process that can influence how cells communicate. Researchers found that while some modifications lead to cell damage or death, others can actually help cells send important signals without harming them. This understanding of how proteins are modified and interact with reactive species is crucial for developing new strategies to treat diseases. Who this helps: This helps doctors and researchers studying cell signaling and disease treatment.

PubMed

Methaemalbumin formation in sickle cell disease: effect on oxidative protein modification and HO-1 induction.

2011

British journal of haematology

Hanson MS, Piknova B, Keszler A, Diers AR, Wang X +3 more

Plain English
This research studied how a substance called methaemalbumin (metHSA) forms in people with sickle cell disease (SCD) and how it affects oxidative stress in their bodies. The researchers found that metHSA can reduce harmful oxidative changes in proteins caused by free hemoglobin, which is often elevated in SCD. However, while metHSA helps limit some damage, it may also reduce the production of a protective enzyme called HO-1 that helps respond to stress in cells. Who this helps: This information is important for doctors and researchers working with sickle cell disease patients.

PubMed

Differential regulation of metabolism by nitric oxide and S-nitrosothiols in endothelial cells.

2011

American journal of physiology. Heart and circulatory physiology

Diers AR, Broniowska KA, Darley-Usmar VM, Hogg N

Plain English
This study investigated how nitric oxide and a related compound called S-nitrosothiol affect energy production in cells that line blood vessels. Researchers found that while nitric oxide mainly reduced the cells' ability to use oxygen, S-nitrosothiol harmed energy production more severely at higher concentrations and affected both energy pathways at different rates. Understanding these effects is important because they shed light on how nitric oxide and similar substances influence blood vessel health. Who this helps: This helps doctors and researchers working on vascular diseases and treatments.

PubMed

Assessing bioenergetic function in response to oxidative stress by metabolic profiling.

2011

Free radical biology & medicine

Dranka BP, Benavides GA, Diers AR, Giordano S, Zelickson BR +7 more

Plain English
This study focused on how cells respond to oxidative stress, which can damage mitochondria and is linked to various diseases like heart issues, diabetes, and cancer. Researchers used advanced techniques to measure how well the mitochondria in living cells function under stress, finding effective ways to monitor changes in their oxygen levels and energy production. This research matters because it helps us understand how oxidative stress affects cell health, which could lead to better treatment strategies for patients with these diseases. Who this helps: This research benefits patients with diseases affected by oxidative stress, such as those with cardiovascular issues, diabetes, and cancer.

PubMed

Mitochondrial targeting of the electrophilic lipid 15-deoxy-Delta12,14-prostaglandin J2 increases apoptotic efficacy via redox cell signalling mechanisms.

2010

The Biochemical journal

Diers AR, Higdon AN, Ricart KC, Johnson MS, Agarwal A +3 more

Plain English
This study looked at a specific lipid called 15-deoxy-Delta12,14-prostaglandin J2 (15d-PGJ2) and its modified version that targets mitochondria, known as mito-15d-PGJ2. Researchers found that mito-15d-PGJ2 was much more effective at causing cell death compared to the original 15d-PGJ2, leading to significant changes in cell energy and signaling. This matters because it shows that targeting treatments to specific parts of cells can improve their effectiveness in killing harmful cells, which could benefit cancer therapies. Who this helps: Patients undergoing cancer treatment.

PubMed

Modulation of mammary cancer cell migration by 15-deoxy-delta(12,14)-prostaglandin J(2): implications for anti-metastatic therapy.

2010

The Biochemical journal

Diers AR, Dranka BP, Ricart KC, Oh JY, Johnson MS +6 more

Plain English
This study examined how a compound called 15d-PGJ2 affects the movement of breast cancer cells, which can contribute to the spread of cancer throughout the body. Researchers found that low doses (between 0.03 and 0.3 microM) of this compound reduced the cells’ ability to migrate and altered their structure in ways that could prevent them from spreading. These findings are important because they suggest that 15d-PGJ2 could be a promising treatment to stop breast cancer from metastasizing without causing harmful side effects. Who this helps: This research benefits breast cancer patients and doctors looking for effective treatments to prevent cancer spread.

PubMed

Homotypic gap junctional communication associated with metastasis suppression increases with PKA activity and is unaffected by PI3K inhibition.

2010

Cancer research

Bodenstine TM, Vaidya KS, Ismail A, Beck BH, Cook LM +3 more

Plain English
This study looked at how cancer cells communicate with each other through tiny channels called gap junctions and how this communication affects cancer spread, or metastasis. Researchers found that two specific drugs increased this communication without affecting another signaling pathway (PI3K), and that the increase in communication was linked to the activity of a protein called PKA. This matters because enhancing cell communication could help reduce how cancer cells spread in the body. Who this helps: This helps patients with cancer by potentially offering new strategies to limit metastasis.

PubMed

Mitochondrial electron transport chain blockers enhance 2-deoxy-D-glucose induced oxidative stress and cell killing in human colon carcinoma cells.

2009

Cancer biology & therapy

Fath MA, Diers AR, Aykin-Burns N, Simons AL, Hua L +1 more

Plain English
Researchers studied how certain drugs that block mitochondrial function (called ETC blockers) can make cancer cells in the colon more sensitive to a sugar blocker called 2-deoxy-D-glucose (2DG). They found that when they combined these blockers with 2DG, there was a significant increase in oxidative stress and cell death in human colon cancer cells. For example, the combination treatment slowed tumor growth in mice, suggesting that using these two types of drugs together could be more effective against colon cancer than using either one alone. Who this helps: This helps patients with colon cancer by providing a potential new treatment strategy.

PubMed

Publication data sourced from PubMed . Plain-English summaries generated by AI. Not medical advice.