Profile

I earned my Ph.D. in Microbiology and did a post-doc on Cancer Biology. For the last several years, my lab has worked on leukemia. A complete understanding of the role of specific regulators (known or novel) in the progression of a disease that can profoundly impact the diagnosis, therapy, and, ultimately, patient survival. We are investigating the molecular mechanisms that delineate CML/AML stem cells from normal hematopoietic stem cells. The research findings may lead to the development of targeted molecular therapies to eliminate the disease before it progresses. Post-translational protein modification is essential in multiple cellular processes, including DNA repair, protein stability, nuclear translocation, protein-protein interactions, cellular proliferation, differentiation, and apoptosis. Multiple post-translational modifications on a protein constitute a complex regulatory program that transduces molecular information to and from signaling pathways. We are investigating whether post-translational modification(s) of EVI1 promote leukemogenesis/oncogenesis.

Current Focus Areas

  • Homing of leukemia stem cells compared to the normal hematopoietic stem cells

  • Mechanism(s) of drug resistance in CML and AML stem cells

  • Consequences of PTBP2 mediated alternative splicing, DNA damage response, and RNA helicases in the progression of CML

  • Transplanted CML and AML model in immune-proficient mice

  • Identification of targets of acetylated and deacetylated EVI1 and decoding their role(s) in leukemogenesis/oncogenesis

  • Dynamics of post-translational modification(s) of EVI1 in metastasis and drug-resistance in colorectal cancer

Selected Publications

  • Agatheeswaran S, Singh S, Biswas S, Biswas G, Chandra Pattnayak N, Chakraborty S. BCR-ABL mediated repression of miR-223 results in the activation of MEF2C and PTBP2 in chronic myeloid leukemia. Leukemia 2013 Jul;27(7):1578-80.

  • Agatheeswaran S and Chakraborty S. MEF2C and CEBPA: possible coregulators in Chronic Myeloid Leukemia disease progression. Int J Biochem Cell Biol. 2016 Aug;77(Pt A):16570.

  • Nayak KB­­, Sajitha I. S., T.R. Santhosh Kumar and Chakraborty S. Ecotropic viral integration site 1 promotes metastasis independent of epithelial mesenchymal transition in colon cancer cells. Cell Death Dis. 2018 Jan 16;9(2):18.

  • Nandagopalan SR, Agatheeswaran S, Vadlamudi Y, Biswas S, Biswas G, Pattnayak NC, Chakraborty S. PTBP2 exon 10 inclusion is associated with the progression of CML and it is BCR-ABL1 dependent. Int J Biochem Cell Biol. 2019 Feb 3;109:69-75.

  • Pradeepa, Suresh V, Singh VK, Nayak KB, Senapati SB, Chakraborty S. EVI1 Promotes Metastasis by Downregulating TIMP2 in Metastatic Colon and Breast Cancer Cells. Int J Biochem Cell Biol. 2022 Jan;142:106118.

Skills & Proficiency

CML AML ALL MDS Colon cancer Post translational modifications RNA binding proteins DNA damage and response Drug resistance Leukemia stem cells