» Articles » PMID: 35176183

Oncogenic and Tumor Suppressor Genes Expression in Myeloproliferative Neoplasms: The Hidden Side of a Complex Pathology

Overview
Journal J Clin Lab Anal
Publisher Wiley
Date 2022 Feb 17
PMID 35176183
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The present study aimed to explore the changes in the expressions of six tumor-related genes in myeloproliferative neoplasms (MPNs). The study population included 130 patients with MPNs (52 with chronic myeloid leukemia (CML), 49 with essential thrombocythemia (ET), 20 with polycythemia vera (PV), and 9 with primary myelofibrosis (PMF)) and 51 healthy individuals.

Methods: The expression profiling of six genes (ADAMTS18, CMTM5, CDKN2B, DCC, FHIT, and WNT5B) in the peripheral blood granulocyte cells was explored by real-time quantitative reverse transcription polymerase chain reaction.

Results: The patients with MPNs showed significant downregulation of CMTM5 (EFC = 0.66) and DCC (EFC = 0.65) genes in contrast to a non-significant upregulation of ADAMTS18, CDKN2B, FHIT, and WNT5B genes. Downregulation of DCC was consistent in all subtypes of MPN (EFC range: 0.591-0.860). However, CMTM5 had a 1.22-fold upregulation in PMF in contrast to downregulation in other MPN subtypes (EFC range: 0.599-0.775). The results revealed a significant downregulation in CMTM5 and DCC at below 60-years of age. Furthermore, female patients showed a clear-cut downregulation in both CMTM5 and DCC (EFC DCC: 0.436 and CMTM5: 0.570), while male patients presented a less prominent downregulation with a borderline p-value only in DCC (EFC: 0.69; p = 0.05).

Conclusions: Chronic myeloid leukemia cases showed a significant upregulation of WNT5B, as a known oncogenesis gene. Two tumor suppressor genes, namely DCC and CMTM5, were downregulated in the patients with MPNs, especially in females and patients below 60 years of age.

Citing Articles

Oncogenic and tumor suppressor genes expression in myeloproliferative neoplasms: The hidden side of a complex pathology.

Abedi E, Karimi M, Yaghobi R, Mohammadi H, Haghpanah S, Moghadam M J Clin Lab Anal. 2022; 36(4):e24289.

PMID: 35176183 PMC: 8993601. DOI: 10.1002/jcla.24289.

References
1.
Shao L, Guo X, Plate M, Li T, Wang Y, Ma D . CMTM5-v1 induces apoptosis in cervical carcinoma cells. Biochem Biophys Res Commun. 2009; 379(4):866-71. DOI: 10.1016/j.bbrc.2008.12.126. View

2.
Gaman M, Cozma M, Dobrica E, Cretoiu S, Gaman A, Diaconu C . Liquid Biopsy and Potential Liquid Biopsy-Based Biomarkers in Philadelphia-Negative Classical Myeloproliferative Neoplasms: A Systematic Review. Life (Basel). 2021; 11(7). PMC: 8304270. DOI: 10.3390/life11070677. View

3.
Barbui T, Thiele J, Gisslinger H, Kvasnicka H, Vannucchi A, Guglielmelli P . The 2016 WHO classification and diagnostic criteria for myeloproliferative neoplasms: document summary and in-depth discussion. Blood Cancer J. 2018; 8(2):15. PMC: 5807384. DOI: 10.1038/s41408-018-0054-y. View

4.
Jiang H, Wang J, Li H, Peng J, Gao X, Chen F . Influence of the DCC gene on proliferation and carcinoembryonic antigen expression in the human colorectal cancer cell line SW1116. Genet Mol Res. 2015; 14(3):10273-80. DOI: 10.4238/2015.August.28.12. View

5.
Ogun Sercan H, Pehlivan M, Simsek O, Ates H, Sercan Z . Induction of apoptosis increases expression of non-canonical WNT genes in myeloid leukemia cell lines. Oncol Rep. 2007; 18(6):1563-9. View