Pubfacts - Scientific Publication Data
  • Categories
  • |
  • Journals
  • |
  • Authors
  • Login
  • Categories
  • Journals

Search Our Scientific Publications & Authors

Publications
  • Publications
  • Authors
find publications by category +
Translate page:

YM155 enhances ABT-737-mediated apoptosis through Mcl-1 downregulation in Mcl-1-overexpressed cancer cells.

Authors:
Seon Min Woo Kyoung-Jin Min Bo Ram Seo Young Ho Seo Yong-Jin Jeong Taeg Kyu Kwon

Mol Cell Biochem 2017 May 24;429(1-2):91-102. Epub 2017 Jan 24.

Department of Immunology, School of Medicine, Keimyung University, 2800 Dalgubeoldaero, Dalseo-Gu, Daegu, 704-701, South Korea.

ABT-737 is a BH3 mimetic inhibitor of Bcl-xL, Bcl-2, and Bcl-w, and it has been reported for anti-cancer effects in various types of cancer cells. However, ABT-737 fails to induce apoptosis in cancer cell with high levels of Mcl-1 expression. The pharmacological survivin inhibitor YM155 has been reported to induce downregulation of Mcl-1 expression. Therefore, we investigated the effect of YM155 to sensitize resistance against ABT-737 in Mcl-1-overexpressed human renal carcinoma Caki cells. We found that ABT-737 alone and YM155 alone did not induce apoptosis, but YM155 markedly sensitized ABT-737-mediated apoptosis in Mcl-1-overexpressed Caki cells, human glioma cells (U251MG), and human lung carcinoma cells (A549). In contrast, combined treatment with ABT-737 and YM155 did not increase apoptosis in normal mouse kidney cells (TCMK-1) and human mesangial cells (MC). YM155 induced lysosome-dependent downregulation of Mcl-1 expression in Mcl-1-overexpressed Caki cells. In addition, combined treatment with ABT-737 and YM155 induced loss of mitochondrial membrane potential and inhibited interaction of Bcl-xL and Bax. Taken together, our results suggested that YM155 effectively improves sensitivity to ABT-737 through downregulation of Mcl-1 expression.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11010-016-2938-0DOI Listing
May 2017

Publication Analysis

Top Keywords

mcl-1 expression
16
downregulation mcl-1
12
abt-737 ym155
12
cells abt-737
12
caki cells
12
ym155
9
cells
9
abt-737-mediated apoptosis
8
ym155 induced
8
mcl-1-overexpressed caki
8
cancer cells
8
induce apoptosis
8
treatment abt-737
8
combined treatment
8
abt-737
7
mcl-1
5
apoptosis
5
human lung
4
u251mg human
4
cells u251mg
4

Similar Publications

Discovery of novel indole-1,2,4-triazole derivatives as tubulin polymerization inhibitors.

Authors:
Meng-Ke Wu Ruo-Jun Man Yan-Juan Liao Hai-Liang Zhu Zhu-Gui Zhou

Drug Dev Res 2021 Mar 6. Epub 2021 Mar 6.

College of Chemistry and Chemical Engineering, Guangxi Key Laboratory of Polysaccharide Materials and Modifications, Guangxi University for Nationalities, Nanning, China.

A series of novel indole-1,2,4-triazole derivatives have been designed, synthesized, and evaluated as potential tubulin polymerization inhibitors. The top hit 12, bearing the 3,4,5-trimethoxyphenyl moiety, exhibited substantial anti-proliferative activity against HepG2, HeLa, MCF-7, and A549 cells in vitro with IC values of 0.23 ± 0. Read More

View Article and Full-Text PDF
March 2021
Similar Publications

Hsa_circ_0110757 upregulates ITGA1 to facilitate temozolomide resistance in glioma by suppressing hsa-miR-1298-5p.

Authors:
Haoyu Li Qing Liu Zihua Chen Ming Wu Chao Zhang Jun Su Yue Li Chi Zhang

Cell Death Dis 2021 Mar 5;12(3):252. Epub 2021 Mar 5.

Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha, 410008, China.

Temozolomide (TMZ) is the internationally recognized and preferred drug for glioma chemotherapy treatment. However, TMZ resistance in glioma appears after long-term use and is an urgent problem that needs to be solved. Circular RNAs (circRNAs) are noncoding RNAs and play an important role in the pathogenesis and progression of tumors. Read More

View Article and Full-Text PDF
March 2021
Similar Publications

Targeting phosphoinositide 3-kinases and histone deacetylases in multiple myeloma.

Authors:
Seiichi Okabe Yuko Tanaka Akihiko Gotoh

Exp Hematol Oncol 2021 Mar 4;10(1):19. Epub 2021 Mar 4.

Department of Hematology, Tokyo Medical University, 6-7-1 Nishi-shinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.

Background: Multiple myeloma (MM) is a type of hematological malignancy affecting the functions of plasma cells. The treatment of MM patients has changed dramatically with the use of new agents. However, unfortunately, it is still incurable. Read More

View Article and Full-Text PDF
March 2021
Similar Publications

Phosphatase PP2A enhances MCL-1 protein half-life in multiple myeloma cells.

Authors:
Anne Slomp Laura M Moesbergen Eric Eldering Marie José Kersten Monique C Minnema Victor Peperzak

Cell Death Dis 2021 Mar 3;12(3):229. Epub 2021 Mar 3.

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Multiple myeloma (MM), a treatable but incurable malignancy, is characterized by the growth of clonal plasma cells in protective niches in the bone marrow. MM cells depend on expression of BCL-2 family proteins, in particular MCL-1, for survival. The regulation of MCL-1 is complex and cell type-dependent. Read More

View Article and Full-Text PDF
March 2021
Similar Publications

The deubiquitinase (DUB) USP13 promotes Mcl-1 stabilisation in cervical cancer.

Authors:
Ethan L Morgan Molly R Patterson Diego Barba-Moreno James A Scarth Adam Wilson Andrew Macdonald

Oncogene 2021 Feb 24. Epub 2021 Feb 24.

School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds, West Yorkshir, UK.

Protein ubiquitination is a critical regulator of cellular homeostasis. Aberrations in the addition or removal of ubiquitin can result in the development of cancer and key components of the ubiquitination machinery serve as oncogenes or tumour suppressors. An emerging target in the development of cancer therapeutics are the deubiquitinase (DUB) enzymes that remove ubiquitin from protein substrates. Read More

View Article and Full-Text PDF
February 2021
Similar Publications
© 2021 PubFacts.
  • About PubFacts
  • Privacy Policy
  • Sitemap