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Inthrani Raja Indran

Researcher at National University of Singapore

Publications -  21
Citations -  1068

Inthrani Raja Indran is an academic researcher from National University of Singapore. The author has contributed to research in topics: Polycystic ovary & Medicine. The author has an hindex of 11, co-authored 17 publications receiving 915 citations.

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Recent advances in apoptosis, mitochondria and drug resistance in cancer cells.

TL;DR: An overview of the recent understanding of apoptotic signaling pathways, the main mechanisms by which cancer cells resist apoptotic insults, and some recent attempts to target the mitochondrion for restoring efficient cell death signaling in cancer cells are provided.
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hTERT overexpression alleviates intracellular ROS production, improves mitochondrial function, and inhibits ROS-mediated apoptosis in cancer cells

TL;DR: It is shown that hTERT overexpression not only reduces the basal cellular reactive oxygen species (ROS) levels but also inhibits endogenous ROS production in response to stimuli that induce intracellular ROS generation, and in doing so endowing cancer cells with the ability to evade death stimuli.
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Preclinical studies and clinical evaluation of compounds from the genus Epimedium for osteoporosis and bone health.

TL;DR: Clinical trials have reported positive effects on bone health, suggesting that compounds or extracts of Epimedium have the potential to be developed as agents, alone or in combination with other drugs, to prevent or delay the onset of osteoporosis and reduce the risk of hip fractures.
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TRAF6 Mediates Suppression of Osteoclastogenesis and Prevention of Ovariectomy-Induced Bone Loss by a Novel Prenylflavonoid.

TL;DR: Novel findings are presented that ICT, by downregulating TRAF6, coordinates inhibition of NF‐κB, MAPK/AP‐1, and ROS signaling pathways to reduce expression and activity of NFATc1.
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A novel prostate cancer therapeutic strategy using icaritin activated arylhydrocarbon-receptor to co-target androgen receptor and its splice variants

TL;DR: It is reported for the first time that a natural prenylflavonoid, icaritin (ICT), can co-target both persistent AR and ARvs, and provide a mechanistic framework for the development of ICT, as a novel lead compound for AR-positive PC therapeutics, especially for those bearing AR splice variants.