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Sabarish Ramachandran

Researcher at Texas Tech University Health Sciences Center

Publications -  46
Citations -  1780

Sabarish Ramachandran is an academic researcher from Texas Tech University Health Sciences Center. The author has contributed to research in topics: Cancer & Mammary tumor. The author has an hindex of 17, co-authored 41 publications receiving 1364 citations. Previous affiliations of Sabarish Ramachandran include Georgia Regents University & Keimyung University.

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Amino Acid Transporters in Cancer and Their Relevance to “Glutamine Addiction”: Novel Targets for the Design of a New Class of Anticancer Drugs

TL;DR: Four amino acid transporters have been found to be expressed at high levels in cancer and show promise in development of new tumor-imaging probes and in tumor-specific delivery of appropriately designed chemotherapeutic agents.
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SLC6A14 (ATB0,+) Protein, a Highly Concentrative and Broad Specific Amino Acid Transporter, Is a Novel and Effective Drug Target for Treatment of Estrogen Receptor-positive Breast Cancer

TL;DR: It is shown that the transporter is up-regulated specifically in estrogen receptor (ER)-positive breast cancer, demonstrable with primary human breast cancer tissues andhuman breast cancer cell lines, and an effective drug target for the treatment of ER- positive breast cancer.
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SIRT1 Is Essential for Oncogenic Signaling by Estrogen/Estrogen Receptor α in Breast Cancer

TL;DR: SIRT1 inactivation eliminated estrogen/ERα-induced cell growth and tumor development, triggering apoptosis and indicated that SIRT1 is required for estrogen-induced breast cancer growth.
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Combined inhibition of DNMT and HDAC blocks the tumorigenicity of cancer stem-like cells and attenuates mammary tumor growth

TL;DR: It is suggested that breast CSCs are intrinsically sensitive to genetic and epigenetic modifications and can therefore be significantly affected by epigenetic-based therapies, warranting further investigation of combined DNMT and HDAC inhibition in refractory or drug-resistant breast cancer.