| Literature DB >> 34355179 |
Bhagyashri Rathod1, Shivam Chak1, Sagarkumar Patel1, Amit Shard1.
Abstract
Pyruvate kinase M2 (PKM2) catalyzes the conversion of phosphoenolpyruvate (PEP) to pyruvate. It plays a central role in the metabolic reprogramming of cancer cells and is expressed in most human tumors. It is essential in indiscriminate proliferation, survival, and tackling apoptosis in cancer cells. This positions PKM2 as a hot target in cancer therapy. Despite its well-known structure and several reported modulators targeting PKM2 as activators or inhibitors, a comprehensive review focusing on such modulators is lacking. Herein we summarize modulators of PKM2, the assays used to detect their potential, the preferable tense (T) and relaxed (R) states in which the enzyme resides, lacunae in existing modulators, and several strategies that may lead to effective anticancer drug development targeting PKM2. This journal is © The Royal Society of Chemistry.Entities:
Year: 2021 PMID: 34355179 PMCID: PMC8292966 DOI: 10.1039/d1md00045d
Source DB: PubMed Journal: RSC Med Chem ISSN: 2632-8682