Debanjan Bhattacharjee
Stanford Medicine, Yale University, Indian Institute of Chemical Technology, University of Calcutta, The University of Burdwan
About
I am a translational oncology researcher whose work focuses on improving the success of oncology drug development by identifying the true mechanisms of action of clinical-stage cancer therapeutics and developing biomarker-guided treatment strategies. I am currently a Postdoctoral Fellow at Stanford Medicine, where my research integrates pharmacogenomics, functional genomics, and mechanistic drug profiling to understand why many oncology drugs fail in clinical trials and how these failures can be addressed through accurate target identification and biomarker-driven patient stratification.
At Stanford Medicine, my research centers on repurposing clinical-stage oncology compounds by uncovering previously unrecognized mechanisms of action. My work on the Phase I compound PAC-1 demonstrated that the drug functions as a selective intracellular iron chelator rather than the originally proposed caspase-3 activator, enabling selective killing of MDR1-high chemotherapy-resistant cancers. This work identified a predictive biomarker for therapeutic response and is helping inform revised clinical trial strategies incorporating biomarker-guided patient selection.
Previously, at Yale School of Medicine, I led a pharmacogenomic and CRISPR-based investigation of the failed Phase II oncology drug ralimetinib. Our study demonstrated that the drug’s anticancer activity is mediated through inhibition of EGFR rather than its originally proposed target, p38α. These findings provided a mechanistic explanation for the drug’s clinical underperformance and highlighted the importance of comprehensive cellular and genetic profiling in accurately understanding drug mechanisms.
My research aims to bridge chemical biology, functional genomics, and clinical oncology to enable rational drug repurposing and precision medicine strategies. I combine high-throughput screening, CRISPR-based functional genomics, biomarker discovery, and preclinical cancer models to identify therapeutically actionable vulnerabilities in drug-resistant cancers.
I received my PhD in Biological Sciences from the CSIR-Indian Institute of Chemical Technology (Hyderabad), where my research focused on cancer drug resistance, chemical biology approaches to targeted protein degradation, and the development of high-throughput screening platforms for anticancer drug discovery. My work has resulted in multiple first-author publications, a patent in drug-resistant cancer therapeutics, and recognition through the Stanford Cancer Institute Early Career Grant.
Employment
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Stanford Medicine Postdoctoral scholar2025 - Present
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Yale University Postdoctoral Research Associate2022 - 2025
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Indian Institute of Chemical Technology Research Technician2014 - 2016
Education
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Indian Institute of Chemical Technology Doctor of Philosophy in Biological Sciences2016 - 2022
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University of Calcutta Masters in Biophysics & Molecular Biology2012 - 2014
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The University of Burdwan Bachelor of Science (Honors)2009 - 2012
Projects & Funding
Projects & funding information is unavailable.
Publications (15)
- A clinical-stage oncology compound selectively targets drug-resistant cancers Save
- Inhibition of a lower potency target drives the anticancer activity of a clinical p38 inhibitor. Save
- A glaucoma-associated OPTN polymorphism, M98K sensitizes retinal cells to endoplasmic reticulum stress and tumour necrosis factor α. Save
- APC/C CDH1 ubiquitinates STAT3 in mitosis. Save
- Plk1 regulates mutant IDH1 enzyme activity and mutant IDH2 ubiquitination in mitosis. Save
- Mutant IDH1 inhibitors activate pSTAT3-Y705 leading to an increase in BCAT1 and YKL-40 levels in mutant IDH1-expressing cells. Save
- APC/C CDH1 ubiquitinates IDH2 contributing to ROS increase in mitosis. Save
- Design, Synthesis, and Biological Evaluation of 2‐(4‐Aminophenyl)benzothiazole Analogues as Antiproliferative Agents Save
- Synthesis and In Vitro Anticancer Activity of Novel 1,3,4‐Oxadiazole‐Linked 1,2,3‐Triazole/Isoxazole Hybrids Save
- Design, Synthesis and Biological Evaluation of 2-Anilinopyridyl-Linked Oxindole Conjugates as Potent Tubulin Polymerisation Inhibitors Save