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Suresh K. Rayala

Researcher at Indian Institute of Technology Madras

Publications -  93
Citations -  3952

Suresh K. Rayala is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Cancer & Kinase. The author has an hindex of 34, co-authored 90 publications receiving 3625 citations. Previous affiliations of Suresh K. Rayala include University of Texas Health Science Center at Houston & University of Texas MD Anderson Cancer Center.

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Importance of functional groups in predicting the activity of small molecule inhibitors for Bcl-2 and Bcl-xL.

TL;DR: This study predicted the factors driving differential activity and specificity implementing multiplexed QSAR analysis for a dataset of 1,649 reported inhibitors of Bcl‐2 (B‐cell lymphoma‐2) and B cl‐xL (B-cell lymphomas‐extra large) and critically analyzed the chemical space with coupling factors.
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Solution structure and antiestrogenic activity of the unique C-terminal, NR-box motif-containing region of MTA1s.

TL;DR: The characterization of structure and antiestrogenic activity of MTA1s peptide highlight its therapeutic potential and finds a predominance of the α-helical region toward the N-terminal region, which includes the NR-box motif.
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Altered localization of a coactivator sensitizes breast cancer cells to tumor necrosis factor–induced apoptosis

TL;DR: It is found that clones of MCF-7 human breast cancer cells overexpressing PELP1 in the cytoplasm were distinctly sensitive to TNF-α-induced apoptosis, paving the way for developing new treatment strategies for tumors with cy toplasmic P ELP1 expression.
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Snail-Modulated MicroRNA 493 Forms a Negative Feedback Loop with the Insulin-Like Growth Factor 1 Receptor Pathway and Blocks Tumorigenesis.

TL;DR: The study showed that nicotine treatment significantly decreases the levels of miR-493—with a concomitant increase in the Levels of Snail—an indication of progression of cells toward tumorigenesis, reestablishing the role of tobacco as a major risk factor for head and neck cancers and elucidating the mechanism behind nicotine-mediated tumorigenisation.
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Identification of a Novel Estrogen Receptor-α Variant and Its Upstream Splicing Regulator

TL;DR: A role for NPE3-3 in alternative splicing is revealed and it is suggested that ERalpha is a physiological target of NPE2-3, leading to a constitutive nongenomic signaling pathway in breast cancer cells.