» Articles » PMID: 26603518

Expression and Regulation of CacyBP/SIP in Chronic Lymphocytic Leukemia Cell Balances of Cell Proliferation with Apoptosis

Overview
Specialty Oncology
Date 2015 Nov 26
PMID 26603518
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: Chronic lymphocytic leukemia (CLL) is the most common leukemia in Western countries, with incidence in Chinese populations also increasing. CLL involves an accumulation of abnormal B cells which result in dysregulation of cell proliferation and apoptosis rates. The calcyclin-binding protein/Siah-1-interacting protein (CacyBP/SIP) plays a pivotal role in tumorigenicity and cell apoptosis. Here, we investigated the function of CacyBP/SIP in CLL cell proliferation and apoptosis.

Methods: CacyBP/SIP expression levels were measured in peripheral blood mononuclear cells from 23 Chinese CLL patients and three healthy donors by western blotting. Correlation analysis was performed to assess associations between CacyBP/SIP expression and clinical stage, chromosome abnormalities and zeta-chain-associated protein kinase 70 (ZAP-70) expression. We silenced CacyBP/SIP expression in MEC-1 cells using a lentivirus system and analyzed cell vitality, cell cycle and tumorigenicity. Apoptosis was also analyzed following the upregulation of CacyBP/SIP expression in MEC-1 cells.

Results: Downregulation of CacyBP/SIP expression in CLL patients was negatively correlated with CLL clinical stage, but not with patient sex, age, del(13q14) or del(17q-) presence, or ZAP-70 expression. CacyBP/SIP silencing significantly enhanced cell proliferation and tumorigenicity. CacyBP/SIP silencing promoted accumulation of cells in S phase by upregulation of β-catenin, cyclin D1 and cyclin E, and downregulation of p21. Moreover, CacyBP/SIP overexpression facilitated CLL apoptosis through the activation of pro-caspase-3.

Conclusion: CacyBP/SIP is a useful indicator of CLL disease processes and plays an important role in sustaining the balance of cell proliferation and apoptosis.

Citing Articles

Pan-analysis reveals CACYBP to be a novel prognostic and predictive marker for multiple cancers.

Mo B, Luo B, Wu Y Am J Transl Res. 2024; 16(1):12-26.

PMID: 38322570 PMC: 10839390.


The multifaceted interactions between Newcastle disease virus proteins and host proteins: a systematic review.

Lu X, Wang X, Liu X, Liu X Virulence. 2024; 15(1):2299182.

PMID: 38193514 PMC: 10793697. DOI: 10.1080/21505594.2023.2299182.


Protective effects of calcyclin-binding protein against pulmonary vascular remodeling in flow-associated pulmonary arterial hypertension.

Zhou J, Li F, Yang Y Respir Res. 2022; 23(1):223.

PMID: 36042446 PMC: 9429705. DOI: 10.1186/s12931-022-02137-z.


Downregulation of CacyBP by CRISPR/dCas9-KRAB Prevents Bladder Cancer Progression.

Zheng H, Chen C Front Mol Biosci. 2021; 8:692941.

PMID: 34179100 PMC: 8226165. DOI: 10.3389/fmolb.2021.692941.


CacyBP/SIP promotes tumor progression by regulating apoptosis and arresting the cell cycle in osteosarcoma.

Zhao M, Zhang R, Qi D, Chen H, Zhang G Exp Ther Med. 2020; 20(2):1397-1404.

PMID: 32742374 PMC: 7388306. DOI: 10.3892/etm.2020.8843.


References
1.
Sun S, Ning X, Liu J, Liu L, Chen Y, Han S . Overexpressed CacyBP/SIP leads to the suppression of growth in renal cell carcinoma. Biochem Biophys Res Commun. 2007; 356(4):864-71. DOI: 10.1016/j.bbrc.2007.03.080. View

2.
Wickremasinghe R, Prentice A, Steele A . p53 and Notch signaling in chronic lymphocytic leukemia: clues to identifying novel therapeutic strategies. Leukemia. 2011; 25(9):1400-7. DOI: 10.1038/leu.2011.103. View

3.
Matsuzawa S, Reed J . Siah-1, SIP, and Ebi collaborate in a novel pathway for beta-catenin degradation linked to p53 responses. Mol Cell. 2001; 7(5):915-26. DOI: 10.1016/s1097-2765(01)00242-8. View

4.
Xia Z, Dai M, Magoulas C, Broxmeyer H, Lu L . Differentially expressed genes during in vitro differentiation of murine embryonic stem cells transduced with a human erythropoietin receptor cDNA. J Hematother Stem Cell Res. 2000; 9(5):651-8. DOI: 10.1089/15258160050196696. View

5.
Chen X, Han G, Zhai H, Zhang F, Wang J, Li X . Expression and clinical significance of CacyBP/SIP in pancreatic cancer. Pancreatology. 2008; 8(4-5):470-7. DOI: 10.1159/000151774. View