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Coral Omene

Researcher at Rutgers University

Publications -  34
Citations -  595

Coral Omene is an academic researcher from Rutgers University. The author has contributed to research in topics: Breast cancer & Medicine. The author has an hindex of 7, co-authored 22 publications receiving 414 citations. Previous affiliations of Coral Omene include New York University.

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Caffeic acid phenethyl ester (CAPE), derived from a honeybee product propolis, exhibits a diversity of anti-tumor effects in pre-clinical models of human breast cancer.

TL;DR: The results strongly suggest that CAPE inhibits MDA-231 and MCF-7 human breast cancer growth via its apoptotic effects, and modulation of NF-κB, the cell cycle, and angiogenesis.
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Caffeic Acid Phenethyl Ester (CAPE) derived from propolis, a honeybee product, inhibits growth of breast cancer stem cells

TL;DR: It is suggested that CAPE causes pronounced changes in bCSC characteristics manifested by inhibition of self renewal, progenitor formation, clonal growth in soft agar, and concurrent significant decrease in CD44 content, all signs of decreased malignancy potential.
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Phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer.

TL;DR: Everolimus-carboplatin was efficacious in metastatic TNBC and dose limiting hematological toxicity was observed when AUC5/6 of carboplatin is combined with everolimus, however, carboplarin AUC 4 was well tolerated in combination with Everolimus with continuing responses.
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Propolis and its Active Component, Caffeic Acid Phenethyl Ester (CAPE), Modulate Breast Cancer Therapeutic Targets via an Epigenetically Mediated Mechanism of Action.

TL;DR: Interestingly, propolis, when normalized for CAPE content, appears to be more potent than CAPE alone similarly to the greater effects of complete foods than isolated components, which provide a potential mechanistic basis for one of the oldest naturopathic agents used in medicine and cancer treatment.
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Clinical and Pharmacologic Differences of CDK4/6 Inhibitors in Breast Cancer.

TL;DR: In this paper, the authors explore the preclinical and pharmacological differences between the three approved agents and help understand the benefits seen with these agents in certain subgroups of patients with metastatic HR positive breast cancer.