Paclitaxel induces inactivation of p70 S6 kinase and phosphorylation of Thr421 and Ser424 via multiple signaling pathways in mitosis

XF Le, WN Hittelman, J Liu, A McWatters, C Li, GB Mills… - Oncogene, 2003 - nature.com
The 70 kDa ribosomal S6 kinase (p70S6K) is important for cell growth and survival.
Activation of p70S6K requires sequential phosphorylation of multiple serine and threonine …

[HTML][HTML] The anti-cancer agent APR-246 can activate several programmed cell death processes to kill malignant cells

Z Wang, H Hu, L Heitink, K Rogers, Y You… - Cell Death & …, 2023 - nature.com
Mutant TP53 proteins are thought to drive the development and sustained expansion of
cancers at least in part through the loss of the wild-type (wt) TP53 tumour suppressive …

p53 and p21 determine the sensitivity of noscapine-induced apoptosis in colon cancer cells

R Aneja, AM Ghaleb, J Zhou, VW Yang, HC Joshi - Cancer research, 2007 - AACR
We have previously discovered the naturally occurring antitussive alkaloid noscapine as a
tubulin-binding agent that attenuates microtubule dynamics and arrests mammalian cells at …

Differential cytotoxicity of clinically important camptothecin derivatives in P-glycoprotein-overexpressing cell lines

Y Hoki, A Fujimori, Y Pommier - Cancer chemotherapy and pharmacology, 1997 - Springer
Camptothecin and its derivatives are specific inhibitors of eukaryotic topoisomerase I (top1)
and are active in cancer patients against a variety of refractory solid tumors and leukemia …

Chk1 and Chk2 are differentially involved in homologous recombination repair and cell cycle arrest in response to DNA double-strand breaks induced by …

M Huang, ZH Miao, H Zhu, YJ Cai, W Lu… - Molecular cancer …, 2008 - AACR
Camptothecins (CPT) activate S or G2-M arrest and the homologous recombination (HR)
repair pathway in tumor cells. In this process, both checkpoint kinases 1 and 2 (Chk1 and …

Gemcitabine-induced activation of checkpoint signaling pathways that affect tumor cell survival

LM Karnitz, KS Flatten, JM Wagner, D Loegering… - Molecular …, 2005 - ASPET
Two signaling pathways are activated by antineoplastic therapies that damage DNA and
stall replication. In one pathway, double-strand breaks activate ataxia-telangiectasia …

Camptothecin analogues with enhanced antitumor activity at acidic pH

DJ Adams, MW Dewhirst, JL Flowers… - Cancer chemotherapy …, 2000 - Springer
Background: Camptothecin (CPT) is a specific inhibitor of the nuclear enzyme
topoisomerase I, which is involved in cellular DNA replication and transcription …

CPT‐11 in human colon‐cancer cell lines and xenografts: characterization of cellular sensitivity determinants

WJM Jansen, B Zwart, STM Hulscher… - … journal of cancer, 1997 - Wiley Online Library
CPT‐11, a new semisynthetic derivative of camptothecin, is active in a number of tumor
types in the clinic, including colon cancer. CPT‐11 is a drug that is converted into the active …

[引用][C] Preclinical and phase I clinical studies with Ckd‐602, a novel camptothecin derivative

JH Lee, JM Lee, KH Lim, JK Kim… - Annals of the New …, 2000 - Wiley Online Library
YOUNG-KYUN KIM, NA-YOUN KOO and PIL-YOUNG YUN, Anticancer effects of CKD-602
(Camtobell®) via G2/M phase arrest in oral squamous cell carcinoma cell lines, Oncology …

Specific activation of the p53 pathway by low dose actinomycin D: a new route to p53 based cyclotherapy

ML Choong, H Yang, MA Lee, DP Lane - Cell cycle, 2009 - Taylor & Francis
The activation of p53 has been proposed as a novel anti-cancer treatment in two distinct
contexts. In the first activation of p53 in tumor cells can promote apoptosis and senescence …