[HTML][HTML] p53 and chemosensitivity

CG Ferreira, C Tolis, G Giaccone - Annals of oncology, 1999 - Elsevier
Background Although hematologic malignancies and some solid tumors such as germ cell
tumors and pediatric malignancies can be cured by cytotoxic treatment, the most prevalent …

Cancer chemoresistance: the relationship between p53 and multidrug transporters

JA Bush, G Li - International journal of cancer, 2002 - Wiley Online Library
Extensive studies indicate that both p53 and multidrug transporters play important roles in
chemoresistance. Since the initial reports a decade ago demonstrating a transcriptional …

Effect of p53 status on sensitivity to platinum complexes in a human ovarian cancer cell line

KE Pestell, SM Hobbs, JC Titley, LR Kelland… - Molecular …, 2000 - ASPET
Wild-type p53 is frequently mutated in late-stage ovarian cancer and has been proposed as
a determinant of cisplatin chemosensitivity. We have therefore established a human ovarian …

Methionine aminopeptidase-2 regulates human mesothelioma cell survival: role of Bcl-2 expression and telomerase activity

A Catalano, M Romano, I Robuffo, L Strizzi… - The American journal of …, 2001 - Elsevier
Methionine aminopeptidase-2 (MetAP2) is the molecular target of the angiogenesis
inhibitors, fumagillin and ovalacin. Fumagillin can also inhibit cancer cell proliferation …

The Impact of p53 Status on Cellular Sensitivity to Antifolate Drugs

X Lu, J Errington, NJ Curtin, J Lunec, DR Newell - Clinical Cancer Research, 2001 - AACR
The impact of p53 status on cellular sensitivity to antifolate drugs has been examined in
seven human cell lines (A549, MCF7, T-47D, CCRF-CEM, COR-L23, A2780, and HCT-116) …

[HTML][HTML] Inhibition of protein kinase CK2 with the clinical-grade small ATP-competitive compound CX-4945 or by RNA interference unveils its role in acute myeloid …

L Quotti Tubi, C Gurrieri, A Brancalion… - Journal of hematology & …, 2013 - Springer
Background The involvement of protein kinase CK2 in sustaining cancer cell survival could
have implications also in the resistance to conventional and unconventional therapies …

Molecular mechanisms of G0/G1 cell‐cycle arrest and apoptosis induced by terfenadine in human cancer cells

JD Liu, YJ Wang, CH Chen, CF Yu… - … in cooperation with …, 2003 - Wiley Online Library
Terfenadine (TF), a highly potent histamine H1 receptor antagonist, has been shown to exert
no significant central nervous system side effects in clinically effective doses. In this study …

Unique dual targeting of thymidylate synthase and topoisomerase1 by FdUMP [10] results in high efficacy against AML and low toxicity

TS Pardee, E Gomes, J Jennings-Gee… - Blood, The Journal …, 2012 - ashpublications.org
Acute myeloid leukemia (AML) is an aggressive malignancy that leads to marrow failure and
death. There is a desperate need for new therapies. The novel fluoropyrimidine, FdUMP …

Global cell proteome profiling, phospho-signaling and quantitative proteomics for identification of new biomarkers in acute myeloid leukemia patients

E Aasebø, RB Forthun, F Berven… - Current …, 2016 - ingentaconnect.com
The identification of protein biomarkers for acute myeloid leukemia (AML) that could find
applications in AML diagnosis and prognosis, treatment and the selection for bone marrow …

Mutation of p53 Gene and Its Correlation with the Clinical Outcome in Dogs with Lymphoma

A Koshino, Y Goto‐Koshino… - Journal of Veterinary …, 2016 - Wiley Online Library
Background p53 plays a key role in the apoptotic event induced by chemotherapeutic
agents. Mutation of p53 gene has been observed in various spontaneous tumors in humans …