Nihal Medatwal
Stony Brook Medicine, University of Pennsylvania Perelman School of Medicine, Amity University Gurugram, National Institute of Immunology, Regional Centre for Biotechnology
Research areas: Biochemistry, Genetics and Molecular Biology · Molecular Biology · Sphingolipid Metabolism and Signaling · Cancer, Lipids, and Metabolism · Nanoparticle-Based Drug Delivery
About
Dr. Nihal Medatwal is an accomplished cancer biologist and lipidomics expert, currently serving as a Postdoctoral Associate in Dr. Yusuf A. Hannun’s Lab at the Cancer Center, Stony Brook Medicine since August 2022. He employs advanced lipidomics platforms, including LC-MS/MS, alongside proteomics, immunoprecipitation, and confocal imaging, to investigate post-translational modifications, protein-protein interactions, and membrane remodeling dynamics.
Prior to joining Stony Brook, Dr. Medatwal was a Postdoctoral Fellow in Dr. Ian A. Blair’s Lab at the University of Pennsylvania, where he contributed to diverse projects including: Comparative lipidomic profiling of monkey and mouse liver tissues, Lung-on-chip studies following chlorine exposure, And biomarker quantification using high-resolution mass spectrometry (HRMS).
Dr. Medatwal earned his Ph.D. in Biotechnology from the Regional Centre for Biotechnology (RCB), India, where his dissertation—titled "Deciphering the Role of Sphingolipids in Cancer Progression and Impact of Chemotherapy on Sphingolipid Signaling"—was mentored by Dr. Avinash Bajaj and Dr. Ujjaini Dasgupta. His doctoral work established critical links between sphingolipid metabolism and cancer cell behavior, including the therapeutic effects of drug combining and evaluating multi-drug treatments impacting sphingolipid-driven tumor progression.
A dedicated and innovative researcher, Dr. Medatwal continues to make impactful contributions to the fields of lipid signaling, cancer biology, and membrane biochemistry, with a long-term vision of translating sphingolipid biology into novel cancer therapeutics.
Employment
-
Stony Brook Medicine Postdoctoral Associate2022 - Present
-
University of Pennsylvania Perelman School of Medicine Post-Doctoral Fellow2021 - 2022
-
Regional Centre for Biotechnology Research scholar2014 - 2021
Education
-
Amity University - Haryana Campus Collaborative work2018 - 2021
-
National Institute of Immunology Colloborative work2017 - 2018
-
Indian Institute of Science Collaborative Work2017 - 2017
- 2014 - 2021
-
University of Rajasthan Master of science2010 - 2012
Projects & Funding
-
Worked in DBT-Funded Institute Department of Biotechnology, Ministry of Science and Technology, India2014 - 2021
Publications (12)
- An integrative approach to studying sphingolipid metabolism reveals p53 as a master regulator of the pathway Save
- A localized hydrogel-mediated chemotherapy causes immunogenic cell death via activation of ceramide-mediated unfolded protein response Save
- Unique sphingolipid signature identifies luminal and triple‐negative breast cancer subtypes Save
- Ceramide Kinase (CERK) Emerges as a Common Therapeutic Target for Triple Positive and Triple Negative Breast Cancer Cells Save
- A hydrogel-based implantable multidrug antitubercular formulation outperforms oral delivery Save
- Alternative splicing of ceramide synthase 2 alters levels of specific ceramides and modulates cancer cell proliferation and migration in Luminal B breast cancer subtype. Save
- Quantitation of Sphingolipids in Mammalian Cell Lines by Liquid Chromatography-Mass Spectrometry Save
- Hydrogel-mediated Delivery of Celastrol and Doxorubicin Induces Synergistic Effect on Tumor Regression via Upregulation of Ceramides Save
- A Localized Chimeric Hydrogel Therapy Combats Tumor Progression through Alteration of Sphingolipid Metabolism Save
- Cholic Acid-Derived Amphiphile which Combats Gram-Positive Bacteria-Mediated Infections via Disintegration of Lipid Clusters Save
- Tethering of Chemotherapeutic Drug/Imaging Agent to Bile Acid-Phospholipid Increases the Efficacy and Bioavailability with Reduced Hepatotoxicity Save
- Molecular Self-Assembly of Bile Acid-Phospholipids Controls the Delivery of Doxorubicin and Mice Survivability Save