Projects per year
Personal profile
Area of Expertise
Dr. Mathew is one of the pioneers who identified, cloned, and characterized several receptors expressed on human NK cells including 2B4 (CD244, SLAMF4), CS1 (CD319, SLAMF7) and LLT1 (CLEC-2D). Research in his laboratory has identified their ligands, elucidated the signaling pathways, and also determined the transcriptional regulation of these genes in health and disease conditions. Dr. Mathew has shown that anti-CS1 antibody activates NK cell cytotoxicity against various cancer cells. The FDA has approved a humanized anti-CS1 mAb, Empliciti, as a breakthrough drug for multiple myeloma treatment. Thus, his research has led to the development of novel NK cell based immunotherapy for cancer. Current focus is identification of markers for cancer stem cells (CSCs) and targeting CSCs to NK cell mediated killing.
Education/Academic qualification
BS in Physics, University of Kerala
MS in Biochemistry, University of Poona
PhD in Biochemistry, University of Poona
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Collaborations and top research areas from the last five years
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Emerging role of tumor-derived
Chaudhary, P. (PI), Mathew, P. (CoI) & Nandy, R. (CoI)
NCI: National Cancer Institute
1/08/23 → 31/07/25
Project: Research
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Exosomal-Annexin A2 Promotes Metastasis in Triple-negative Breast Cancer
Chaudhary, P. (PI) & Mathew, P. (CoI)
1/06/17 → 31/05/18
Project: Research
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Molecular Characterization of NKp44 Ligand on Astrocytes
Mathew, P. (PI) & Mathew, S. (CoI)
NINDS: Neurological Disorders & Stroke
1/02/17 → 31/01/19
Project: Research
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Molecular Characterization of NKp44 Ligand on Astrocytes
Mathew, P. (PI)
National Institute of Neurological Disorders and Stroke
1/02/17 → 31/01/20
Project: Research
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Molecular Characterization of NKp44 Ligand on Astrocytes
Mathew, P. (PI)
1/02/17 → 31/01/20
Project: Research
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Requirement of homotypic NK-cell interactions through 2B4(CD244)/CD48 in the generation of NK effector functions
Lee, K. M., Forman, J. P., McNerney, M. E., Stepp, S., Kuppireddi, S., Guzior, D., Latchman, Y. E., Sayegh, M. H., Yagita, H., Park, C. K., Seog, B. O., Wülfing, C., Schatzle, J., Mathew, P. A., Sharpe, A. H. & Kumar, V., 15 Apr 2006, In: Blood. 107, 8, p. 3181-3188 8 p.Research output: Contribution to journal › Article › peer-review
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Role of LLT1 and PCNA as Natural Killer Cell Immune Evasion Strategies of HCT 116 Cells
Malaer, J. D. & Mathew, P. A., Dec 2020, In: Anticancer Research. 40, 12, p. 6613-6621 9 p.Research output: Contribution to journal › Article › peer-review
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The LLT1 receptor induces IFN-γ production by human natural killer cells
Mathew, P. A., Chuang, S. S., Vaidya, S. V., Kumaresan, P. R., Boles, K. S. & Pham, H. T. K., Mar 2004, In: Molecular Immunology. 40, 16, p. 1157-1163 7 p.Research output: Contribution to journal › Article › peer-review
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“Designer Membranes”: Construction of a Cell Containing Multiple Membrane-Bound Cytochromes P450
Estabrook, R. W., Trant, J. M., Mathew, P. A., Mason, J. I. & Waterman, M. R., 1 Jan 1992, Current Topics in Cellular Regulation. C ed. p. 419-431 13 p. (Current Topics in Cellular Regulation; vol. 33, no. C).Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review
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Amino acid substitutions Phe66 → Leu and Ser126 → Pro abolish cortisol and aldosterone synthesis by bovine cytochrome P45011β
Mathew, P. A., Mason, J. I., Trant, J. M., Sanders, D. & Waterman, M. R., 25 Nov 1990, In: Journal of Biological Chemistry. 265, 33, p. 20228-20233 6 p.Research output: Contribution to journal › Article › peer-review