mRNA Expression and DNA Methylation of CXCL16 in Menstrual Blood and Endometrium Tissue of Subjects with Endometriosis and Pelvic Pain
Abstract
BACKGROUND: The cytokine chemokine ligand 16 (CXCL16) plays an important role in the pathophysiology of endometriosis by regulating the inflammatory response and contributing to the pain-associated endometriosis. Despite this, the impact of epigenetic modifications, such as DNA methylation, on CXCL16 has yet to be fully understood. Therefore, this research was conducted to assess both the mRNA expression and DNA methylation levels of the proinflammatory gene CXCL16 in the endometrium tissue and menstrual blood of patients with and without endometriosis.
METHODS: Thirty-five women with and without endometriosis were involved in this research. Subjects' menstrual blood samples were collected using filter paper pads, meanwhile the endometrium tissue were collected by performing biopsy, from which DNA and RNA were extracted. The DNA methylation levels of the CXCL16 were measured using the pyrosequencing method following bisulfite conversion treatment. Meanwhile, the mRNA expression level was measured using the quantitative polymerase chain reaction (qPCR) method and analyzed with the Livak method.
RESULTS: The mRNA expression of CXCL16 in menstrual blood of endometriosis subjects was 2.42 times higher compared to control group (p=0.030). Furthermore, the expression of CXCL16 in menstrual blood was identical to that in endometrial tissue (p=0.173). DNA methylation analysis showed that CXCL16 in the menstrual blood of endometriosis subjctes had lower methylation levels compared to controls (p=0.004), indicating hypomethylation.
CONCLUSION: Increased mRNA expression and hypomethylation of CXCL16 in the menstrual blood of endometriosis patients could serve as a direct marker for diagnosing endometriosis. However, further study to validate these findings and explore the potential of CXCL16 as a diagnostic tool, and additional research involving larger patient for the cohorts study is necessary.
KEYWORDS: CXCL16, DNA methylation, endometrium, menstrual blood, mRNA expression, pain
References
Yuane E, Dewanto A, Widad S. High expression of PR-A and low expression of PR-B is correlated with inflammation in endometrioma cases. Indones Biomed J. 2023; 15(1): 85-93, CrossRef.
Sari V, Jenie RI, Widad S, Dewanto A. MMP-9 and TIMP-1 promote extracellular matrix remodeling in the formation of ovarian endometrioma: in vitro study on chicken chorioallantoic membrane. Indones Biomed J. 2023; 15(1): 69-76, CrossRef.
Saragih CF, Rivany R, Sahil MF, Fadjrir F, Ardiansyah E, Yaznil MR, et al. The difference of Bax protein expression between endometrioma and ovarian carcinoma. Mol Cell Biomed Sci. 2019; 3(2): 95-9, CrossRef.
Gupta S, Harlev A, Agarwal A, Pandithurai E. Theories on endometriosis. In: Gupta S, Harlev A, Agarwal A, editors. Endometriosis: A Comprehensive Update. Cham: Springer; 2015. p.17-21, CrossRef.
Eisenberg V, Weil C, Chodick G, Shalev V. Epidemiology of endometriosis: A large population-based database study from a healthcare provider with 2 million members. BJOG. 2018; 125(1): 55-62, CrossRef.
Hestiantoro A, Natadisastra RM, Sumapraja K, Wiweko B, Pratama G, Situmorang H, et al. Best Practice on IMPERIAL. Jakarta: CV Sagung Seto; 2012.
Gupta S, Harlev A, Agarwal A, Pandithurai E, Cirenza C. Introduction to endometriosis. In: Gupta S, Harlev A, Agarwal A, editors. Endometriosis: A Comprehensive Update. Cham: Springer; 2015. p.1-5, CrossRef.
Sourial S, Tempest N, Hapangama DK. Theories on the pathogenesis of endometriosis. Int J Reprod Med. 2014; 2014: 179515, CrossRef.
Peng Y, Ma J, Lin J. Activation of the CXCL16/CXCR6 axis by TNF-a contributes to ectopic endometrial stromal cells migration and invasion. Reprod Sci. 2019; 26(3): 420-7, CrossRef.
Naura NF. Correlation Analysis of DNA Methylation and mRNA Expression of Nerve Growth Factor (NGF) in Menstrual Blood Samples of Women with Endometiosis [Essay]. Jakarta: Universitas Indonesia; 2020, article.
Yang H, Zhou B, Prinz M, Siegel D. Proteomic analysis of menstrual blood. Mol Cell Proteomics. 2012; 11(10): 1024-35, CrossRef.
Koukoura O, Sifakis S, Spandidos DA. DNA methylation in endometriosis (Review). Mol Med Rep. 2016; 13(4): 2939-48, CrossRef.
Yudiyanta, Khoirunnisa N, Novitasari RW. Assessment nyeri. Cermin Dunia Kedokt. 2015; 42(3): 214-34, article.
Poulin M, Zhou JY, Yan L, Shioda T. Pyrosequencing methylation analysis. In: Dumitrescu RG, Verma M, editors. Cancer Epigenetics for Precision Medicine: Methods and Protocols. Totowa, NJ: Humana Press; 2018. p.283-96, CrossRef.
Mihm M, Gangooly S, Muttukrishna S. The normal menstrual cycle in women. Anim Reprod Sci. 2011; 124(3-4): 229-36, CrossRef.
Houshdaran S, Nezhat CR, Vo KC, Zelenko Z, Irwin JC, Giudice LC. Aberrant endometrial DNA methylome and associated gene expression in women with endometriosis. Biol Reprod. 2016; 95(5): 93, CrossRef.
Brosens I, Brosens JJ, Benagiano G. The eutopic endometrium in endometriosis: Are the changes of clinical significance? Reprod Biomed Online. 2012; 24(5): 496-502, CrossRef.
Deaton AM, Bird A. CpG islands and the regulation of transcription. Genes Dev. 2011; 25(10): 1010-22, CrossRef.
Cai Y. Review of CpG island recognition algorithms. J Phys Conf Ser. 2020; 1624: 042026, CrossRef.
Portela A, Esteller M. Epigenetic modifications and human disease. Nat Biotechnol. 2010; 28(10): 1057-68, CrossRef.
Amstrong L. Epigenetics. New York, NY : Garland Science/Taylor & Francis Group, 2014, NLMID.
Wang Y, Nicholes K, Shih IM. The origin and pathogenesis of endometriosis. Annu Rev Pathol. 2020; 15: 71-95, CrossRef.
Hikmawati N, Hestiantoro A, Muharam R, Marwali ML, Surur A, Aninditha T, et al. Analysis of DNA methylation level and mRNA expression of transient receptor ankyrin member 1 (TRPA1) in endometriosis-associated pain. Asia Pac J Mol Biol Biotechnol. 2021; 29(3): 1-10, CrossRef.
Babaabasi B, Ahani A, Sadeghi F, Bashizade-Fakhar H, Khorshid HRK. The association between TNF-alpha gene polymorphisms and endometriosis in an Iranian population. Int J Fertil Steril. 2019; 13(1): 6-11, CrossRef.
Garcia-Gomez E, Vazquez-Martinez ER, Reyes-Mayoral C, Cruz-Orozco OP, Camacho-Arroyo I, Cerbon M. Regulation of inflammation pathways and inflammasome by sex steroid hormones in endometriosis. Front Endocrinol. 2019; 10: 935, CrossRef.
Shao X, Yang X, Shen J, Chen S, Jiang X, Wang Q, Di W. TNF-alpha-induced p53 activation induces apoptosis in neurological injury. J Cell Mol Med. 2020; 24(12): 6796-803, CrossRef.
Morotti M, Vincent K, Becker CM. Mechanisms of pain in endometriosis. Eur J Obstet Gynecol Reprod Biol. 2017; 209: 8-13, CrossRef.
Gruber TM, Mechsner S. Pathogenesis of endometriosis: The origin of pain and subfertility. Cells. 2021; 10(6): 1381, CrossRef.
Manabe S, Iwase A, Goto M, Kobayashi H, Takikawa S, Nagatomo Y, et al. Expression and localization of CXCL16 and CXCR6 in ovarian endometriotic tissues. Arch Gynecol Obstet. 2011; 284(6): 1567-72, CrossRef.
Peng Y, Ma J, Lin J. Activation of the CXCL16/CXCR6 axis by TNF-α contributes to ectopic endometrial stromal cells migration and invasion. Reprod Sci. 2019; 26(3):420-7, CrossRef.
DOI: https://doi.org/10.18585/inabj.v16i2.2958
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