Mechanisms for the activity of heterocyclic cyclohexanone curcumin derivatives in estrogen receptor negative human breast cancer cell lines

TJ Somers-Edgar, S Taurin, L Larsen… - Investigational new …, 2011 - Springer
Estrogen receptor (ER)-negative breast cancer is an aggressive form that currently requires
more drug treatment options. Thus, we have further modified cyclohexanone derivatives of …

[HTML][HTML] RL71, a second-generation curcumin analog, induces apoptosis and downregulates Akt in ER-negative breast cancer cells

B Yadav, S Taurin, L Larsen… - … journal of oncology, 2012 - spandidos-publications.com
There is a need for the development of new, safe and efficacious drug therapies for the
treatment of estrogen receptor (ER)-negative breast cancers. RL71 is a second-generation …

New bis (hydroxymethyl) alkanoate curcuminoid derivatives exhibit activity against triple-negative breast cancer in vitro and in vivo

MT Hsieh, LC Chang, HY Hung, HY Lin… - European Journal of …, 2017 - Elsevier
Novel bis (hydroxymethyl) alkanoate curcuminoid derivatives were designed, synthesized
and screened for in vitro antiproliferative and in vivo antitumor activity. Selected new …

Synthesis and cytotoxic potential of heterocyclic cyclohexanone analogues of curcumin

B Yadav, S Taurin, RJ Rosengren… - Bioorganic & medicinal …, 2010 - Elsevier
A series of 18 heterocyclic cyclohexanone analogues of curcumin have been synthesised
and screened for their activity in both adherent and non-adherent cancer cell models …

RL66 a second-generation curcumin analog has potent in vivo and in vitro anticancer activity in ER‑negative breast cancer models

B Yadav, S Taurin, L Larsen… - … journal of oncology, 2012 - spandidos-publications.com
There is a need for the development of new safe and efficacious drug therapies for the
treatment of estrogen receptor (ER)‑negative breast cancers. 1-Methyl-3, 5-bis [(E)-4-pyridyl) …

Synthesis of curcumin derivatives and analysis of their antitumor effects in triple negative breast cancer (TNBC) cell lines

PM Bonaccorsi, M Labbozzetta, A Barattucci… - Pharmaceuticals, 2019 - mdpi.com
We analyzed antitumor effects of a series of curcumin analogues. Some of them were
obtained by reaction of substitution involving the two phenolic OH groups of curcumin while …

[PDF][PDF] Antiproliferative effect of an analog of curcumin bis-1, 7-(2-hydroxyphenyl)-hepta-1, 6-diene-3, 5-dione in human breast cancer cells.

M Kumaravel, P Sankar… - European Review for …, 2012 - europeanreview.org
MATERIALS AND METHODS: We compared the impact of bis-1, 7-2 (hydroxyphenil)-hepta-
1, 6diene-3, 5diore (BDMC-A) with that of curcumin in human breast cancer cell line MCF-7 …

Curcumin exerts multiple suppressive effects on human breast carcinoma cells

ZM Shao, ZZ Shen, CH Liu… - … journal of cancer, 2002 - Wiley Online Library
In our study, we present experimental evidence suggesting that curcumin exerts multiple
different suppressive effects on human breast carcinoma cells in vitro. Our experiments …

Recent advances of curcumin derivatives in breast cancer

Y Yin, Y Tan, X Wei, X Li, H Chen, Z Yang… - Chemistry & …, 2022 - Wiley Online Library
Curcumin is a potential plant‐derived drug for the treatment of breast cancer. Poor solubility
and bioavailability are the main factors that limit its clinical application. Various structural …

Curcumin analog B14 has high bioavailability and enhances the effect of anti‐breast cancer cells in vitro and in vivo

H Shen, J Shen, H Pan, L Xu, H Sheng, B Liu… - Cancer …, 2021 - Wiley Online Library
Curcumin has a variety of anticancer properties, but low bioavailability prevents its use in
chemotherapeutic applications. To address this problem, we tested the efficacy of the …