Literature DB >> 28548025

Reprogramming the oncogenic response: SET protein as a potential therapeutic target in cancer.

Man-Hsin Hung1,2, Kuen-Feng Chen3.   

Abstract

INTRODUCTION: SET is a multitask oncoprotein that promotes the initiation and progression of cancer. Overexpression of SET has been characterized as being tumor-specific and is associated with adverse clinical outcomes in many different human malignant diseases. Notably, SET has been shown to promote the development of therapeutic resistance in cancer cells. Area covered: In this review, we summarized the currently available evidence relating to the oncogenic roles, biological functions and clinical relevance of SET protein in cancer. The anti-cancer effects of three different SET antagonists undergoing preclinical investigation are also discussed. Expert opinion: Emerging evidence supports the critical role of SET in regulating various different cancer hallmarks. Targeting the SET-associated protein interfaces may be a potential anti-cancer strategy for future development. However, more studies are required to clarify the best strategy to combine SET antagonists with other anti-cancer treatments and to explore possible biomarkers that predict responsiveness.

Entities:  

Keywords:  PP2A; SET; cancer; oncoprotein; target therapy

Mesh:

Substances:

Year:  2017        PMID: 28548025     DOI: 10.1080/14728222.2017.1336226

Source DB:  PubMed          Journal:  Expert Opin Ther Targets        ISSN: 1472-8222            Impact factor:   6.902


  12 in total

Review 1.  Functioning mechanisms of Shugoshin-1 in centromeric cohesion during mitosis.

Authors:  Qian Zhang; Hong Liu
Journal:  Essays Biochem       Date:  2020-09-04       Impact factor: 8.000

2.  Isolation of Primary Hepatocytes for Testing Tumor Penetrating Peptides.

Authors:  Eric Savier; Pierre Tuffery; Heriberto Bruzzoni-Giovanelli; Angelita Rebollo
Journal:  Methods Mol Biol       Date:  2022

3.  SET/PP2A signaling regulates macrophage positioning in hypoxic tumor regions by amplifying chemotactic responses.

Authors:  Shaolong Zhang; Jingping Zhou; Pengzhao Shang; Guomeng Zhao; Anlei Wang; Jinlei Mao; Yuhang Tao; Ziyi Chen; Xuehao Wang; Changying Guo
Journal:  Exp Mol Med       Date:  2022-10-12       Impact factor: 12.153

4.  Upregulated SET Promotes Cell Survival Through Activating Akt/NF-κB Signal in Colorectal Carcinoma.

Authors:  Jianjun Zhu; Lihong Shi; Genlai Du; Li Li; Ming Liu
Journal:  Cancer Manag Res       Date:  2020-06-19       Impact factor: 3.989

5.  Cyclin-dependent kinase 1-mediated phosphorylation of SET at serine 7 is essential for its oncogenic activity.

Authors:  Ling Yin; Yongji Zeng; Yi Xiao; Yuanhong Chen; Hong Shen; Jixin Dong
Journal:  Cell Death Dis       Date:  2019-05-16       Impact factor: 8.469

6.  SET binding to Sgo1 inhibits Sgo1-cohesin interactions and promotes chromosome segregation.

Authors:  Qianhui Qu; Qian Zhang; Lu Yang; Yujue Chen; Hong Liu
Journal:  J Cell Biol       Date:  2019-06-21       Impact factor: 10.539

Review 7.  Protein phosphatase 2A as a therapeutic target in inflammation and neurodegeneration.

Authors:  Andrew R Clark; Michael Ohlmeyer
Journal:  Pharmacol Ther       Date:  2019-06-01       Impact factor: 12.310

8.  Oncogenic Roles Of A Histone Methyltransferase SETDB2 In AML1-ETO Positive AML.

Authors:  Guangfu Mu; Fangping Chen
Journal:  Cancer Manag Res       Date:  2020-02-04       Impact factor: 3.989

9.  SET levels contribute to cohesion fatigue.

Authors:  Lu Yang; Qian Zhang; Tianhua Niu; Hong Liu
Journal:  Mol Biol Cell       Date:  2021-04-28       Impact factor: 4.138

10.  Targeting of SET/I2PP2A oncoprotein inhibits Gli1 transcription revealing a new modulator of Hedgehog signaling.

Authors:  Iliana Serifi; Simoni Besta; Zoe Karetsou; Panagiota Giardoglou; Dimitris Beis; Pawel Niewiadomski; Thomais Papamarcaki
Journal:  Sci Rep       Date:  2021-07-06       Impact factor: 4.379

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