Rottlerin potentiates camptothecin-induced cytotoxicity in human hormone refractory prostate cancers through increased formation and stabilization of topoisomerase I …

JL Hsu, YF Ho, TK Li, CS Chen, LC Hsu… - Biochemical …, 2012 - Elsevier
Combination therapy, which can optimize killing activity to cancers and minimize drug
resistance, is a mainstream therapy against hormone-refractory prostate cancers (HRPCs) …

Dual action of NSC606985 on cell growth and apoptosis mediated through PKCδ in prostatic cancer cells

X Wang, C Tan, G Wang, JJ Cai… - International …, 2017 - spandidos-publications.com
Chemotherapy is a vital therapeutic strategy for castration-resistant prostate cancer (CRPC).
We have previously shown that NSC606985 (NSC), a camptothecin (CPT) analog, induced …

CFS-1686 causes cell cycle arrest at intra-S phase by interference of interaction of topoisomerase 1 with DNA

RW Lin, CN Yang, SY Ku, CJ Ho, SB Huang… - PLoS …, 2014 - journals.plos.org
CFS-1686 (chemical name (E)-N-(2-(diethylamino) ethyl)-4-(2-(2-(5-nitrofuran-2-yl) vinyl)
quinolin-4-ylamino) benzamide) inhibits cell proliferation and triggers late apoptosis in …

Rottlerin promotes anti-metastatic events by ameliorating pharmacological parameters of paclitaxel: An in-vivo investigation in the orthotopic mouse model of breast …

D Manhas, KB Mir, N Tripathi, S Bharti… - Chemico-Biological …, 2022 - Elsevier
Despite substantial breakthroughs in cancer research, there is hardly any specific therapy
available to date that can alleviate triple-negative breast cancer (TNBC). Paclitaxel is the first …

Multiple mechanisms of Rottlerin toxicity in A375 melanoma cells

F Ietta, G Valacchi, L Benincasa, A Pecorelli… - …, 2019 - Wiley Online Library
Rottlerin is a cytostatic and cytotoxic drug in a variety of cancer cells. Our previous
experience demonstrated that depending upon the genetic/biochemical background of …

Mechanistic study of dual‐function inhibitors targeting topoisomerase II and Rad51‐mediated DNA repair pathway against castration‐resistant prostate cancer

YC Chiang, WJ Leu, YC Chen, PC Ye, YT Hsu… - The …, 2023 - Wiley Online Library
Background Castration‐resistant prostate cancer (CRPC) is refractory to hormone treatment
and the therapeutic options are continuously advancing. This study aims to discover the anti …

Induction of DNA damage and ATF3 by retigeric acid B, a novel topoisomerase II inhibitor, promotes apoptosis in prostate cancer cells

Y Liu, F Gao, H Jiang, L Niu, Y Bi, CYF Young, H Yuan… - Cancer letters, 2013 - Elsevier
Retigeric acid B (RB) has been reported to exhibit its anti-tumor activity in vitro and in vivo.
Here, we found that RB significantly inhibited activity of topoisomerase IIα (Topo IIα), leading …

Neutral porphyrin derivative exerts anticancer activity by targeting cellular topoisomerase I (Top1) and promotes apoptotic cell death without stabilizing Top1-DNA …

SK Das, A Ghosh, S Paul Chowdhuri… - Journal of Medicinal …, 2018 - ACS Publications
Camptothecin (CPT) selectively traps topoisomerase 1-DNA cleavable complexes (Top1cc)
to promote anticancer activity. Here, we report the design and synthesis of a new class of …

Down-regulation of caspase-2 by rottlerin via protein kinase C-δ–independent pathway

A Basu, B Adkins, C Basu - Cancer Research, 2008 - AACR
Protein kinase C-δ (PKCδ) plays an important role in DNA damage–induced apoptosis. We
have previously shown that the PKCδ inhibitor rottlerin protects against cisplatin-induced …

Topoisomerase IIβ–mediated DNA double-strand breaks: implications in doxorubicin cardiotoxicity and prevention by dexrazoxane

YL Lyu, JE Kerrigan, CP Lin, AM Azarova, YC Tsai… - Cancer research, 2007 - AACR
Doxorubicin is among the most effective and widely used anticancer drugs in the clinic.
However, cardiotoxicity is one of the life-threatening side effects of doxorubicin-based …