Article Data

  • Views 523
  • Dowloads 129

Original Research

Open Access

A correlational study on MiR-34s and cervical lesions

  • Xiaowan Liu1
  • Zhen Jiao1
  • Hongxiang Chen1
  • LingWang1,*,

1Department of Gynaecology, People’s Hospital of Xinjiang Uygur Autonomous Region, Urumqi, Xinjiang (China)

DOI: 10.12892/ejgo4405.2018 Vol.39,Issue 5,October 2018 pp.786-789

Published: 10 October 2018

*Corresponding Author(s): LingWang E-mail: cnxiaowanliu@163.com

Abstract

Objective: The aims of this study were to explore the correlation between MiR-34s and cervical lesions. Materials and Methods: A casecontrol study was conducted. From 2014 to 2015, 120 cases were included and divided into four groups depending on cervical biopsy, including group 0 (cervicitis or normal cervix), group 1 (CINI), group 2 (CINII-III), and group C (cervical cancer); each group included 30 cases. Then the relationship between miRNA-34 family (including miRNA-34a, miRNA-34b, miRNA-34c) and clinical pathological features was analysed based on detection of miRNA-34 by real-time polymerase chain reaction (RT-PCR). Results: The expression level of miRNA-34a in group 0 was 0.19 ± 0.1073, in group 1 it was 0.1507 ±0. 2124, in group 2 it was 0.0766 ± 0.0948 (vs. group 0: p < 0.05), and in group C it was 0.0501 ± 0.0271 (vs. Group 0: p < 0.05). The correlation analysis showed that the expression of miRNA-34a decreased with the aggravating of the cervical lesion (r = -0.4782, p < 0.05), while there was no difference of miRNA-34b (F = 0.5835, p = 0.6282) or miRNA-34c (F = 0.1167, p = 0.9500) in each group. Conclusion: The decrease of miRNA-34a is related with cervical malignant lesion, which may be involved in the pathogenesis by regulating target genes, that may be a new molecular marker for diagnosis and prognosis of cervical cancer.

Keywords

miRNA-34s; Cervical lesions; Cervical cancer.

Cite and Share

Xiaowan Liu,Zhen Jiao,Hongxiang Chen,LingWang. A correlational study on MiR-34s and cervical lesions. European Journal of Gynaecological Oncology. 2018. 39(5);786-789.

References

[1] Sadalla J.C., Andrade J.M., Genta M.L., Baracat E.C.: “Cervical cancer: what’s new?” Rev. Assoc. Med. Bras. (1992), 2015, 61, 536.

[2] McGuire S.: “World Cancer Report 2014. Geneva, Switzerland: World Health Organization, International Agency for Research on Cancer, WHO Press, 2015”. Adv. Nutr., 2016, 7, 418.

[3] Lorenzi A.T., Fregnani J.H., Possati-Resende J.C., Neto C.S., Villa L.L., Longatto-Filho A.: “Self-collection for high-risk HPV detection in Brazilian women using the careHPV™ test”. Gynecol. Oncol., 2013, 131, 131.

[4] Campos N.G., Sharma M., Clark A., Kim J.J., Resch S.C.: “Resources Required for Cervical Cancer Prevention in Low- and Middle-Income Countries”. PLoS One, 2016, 11, e0164000.

[5] Origoni M., Salvatore S., Perino A., Cucinella G., Candiani M.: “Cervical Intraepithelial Neoplasia (CIN) in pregnancy: the state of the art”. Eur. Rev. Med. Pharmacol. Sci., 2014, 18, 851.

[6] Somashekhar S.P., Ashwin K.R.: “Management of Early Stage Cervical Cancer”. Rev. Recent. Clin. Trials., 2015, 10, 302.

[7] Wang F., Li B., Xie X.: “The roles and clinical significance of microRNAs in cervical cancer”. Histol. Histopathol., 2016, 31, 131.

[8] Ribeiro J., Sousa H.: “MicroRNAs as biomarkers of cervical cancer development: a literature review on miR-125b and miR-34a”. Mol. Biol. Rep., 2014, 41, 1525.

[9] Siemens H., Jackstadt R., Hünten S., Kaller M., Menssen A., Götz U., et al.: “miR-34 and SNAIL form a double-negative feedback loop to regulate epithelial-mesenchymal transitions”. Cell Cycle, 2011, 10, 4256.

[10] Agostini M., Knight R.A.: “miR-34: from bench to bedside”. Oncotarget, 2014, 5, 872.

[11] Hermeking H.: “The miR-34 family in cancer and apoptosis”. Cell Death Differ., 2010, 17, 193.

[12] Goh A.M., Coffill C.R., Lane D.P.: “The role of mutant p53 in human cancer”. J. Pathol., 2011, 223, 116.

[13] Bianchi E., Ruberti S., Rontauroli S., Guglielmelli P., Salati S., Rossi C., et al.: “Role of miR-34a-5p in Hematopoietic Progenitor Cells Proliferation and Fate Decision: Novel Insights into the Pathogenesis of Primary Myelofibrosis”. Int. J. Mol. Sci., 2017, 18, E145.

[14] Yang B.H., Bray F.I., Parkin D.M., Sellors J.W., Zhang Z.F.: “Cervical cancer as a priority for prevention in different world regions: an evaluation using years of life lost”. Int. J. Cancer, 2004, 109, 418.

[15] Fang J., Zhang H., Jin S.: “Epigenetics and cervical cancer: from pathogenesis to therapy”. Tumour Biol., 2014, 35, 5083.

[16] Petry K.U.: “HPV and cervical cancer”. Scand. J. Clin. Lab. Invest. Suppl., 2014, 244, 59.

[17] Goodman A.: “HPV testing as a screen for cervical cancer”. BMJ, 2015, 350, h2372.

[18] Mohr A.M., Mott J.L.: “Overview of microRNA biology”. Semin. Liver Dis., 2015, 35, 3.

[19] Lau N.C., Lim L.P., Weinstein E.G., Bartel D.P.: “An abundant class of tiny RNAs with probable regulatory roles in Caenorhabditis elegans”. Science, 2001, 294, 858.

[20] Song R., Walentek P., Sponer N., Klimke A., Lee J.S., Dixon G., et al.: “miR-34/449 miRNAs are required for motile ciliogenesis by repressing cp110”. Nature, 2014, 510, 115.

[21] Wong K.Y., Yu L., Chim C.S.: “DNA methylation of tumor suppressor miRNA genes: a lesson from the miR-34 family”. Epigenomics, 2011, 3, 83.

[22] O’Day E., Lal A.: “MicroRNAs and their target gene networks in breast cancer”. Breast Cancer Res., 2010, 12, 201.

[23] Li Y., Guessous F., Zhang Y., Dipierro C., Kefas B., Johnson E., et al.: “MicroRNA-34a inhibits glioblastoma growth by targeting multiple oncogenes”. Cancer Res., 2009, 69, 7569.

[24] Pang R.T., Leung C.O., Ye T.M., Liu W., Chiu P.C., Lam K.K., et al.: “MicroRNA-34a suppresses invasion through downregulation of Notch1 and Jagged1 in cervical carcinoma and choriocarcinoma cells”. Carcinogenesis, 2010, 31, 1037.

[25] Hagman Z., Haflidadottir B.S., Ansari M., Persson M., Bjartell A., Edsjö A., et al.: “The tumour suppressor miR-34c targets MET in prostate cancer cells”. Br. J. Cancer, 2013, 109, 1271.

Abstracted / indexed in

Science Citation Index Expanded (SciSearch) Created as SCI in 1964, Science Citation Index Expanded now indexes over 9,500 of the world’s most impactful journals across 178 scientific disciplines. More than 53 million records and 1.18 billion cited references date back from 1900 to present.

Biological Abstracts Easily discover critical journal coverage of the life sciences with Biological Abstracts, produced by the Web of Science Group, with topics ranging from botany to microbiology to pharmacology. Including BIOSIS indexing and MeSH terms, specialized indexing in Biological Abstracts helps you to discover more accurate, context-sensitive results.

Google Scholar Google Scholar is a freely accessible web search engine that indexes the full text or metadata of scholarly literature across an array of publishing formats and disciplines.

JournalSeek Genamics JournalSeek is the largest completely categorized database of freely available journal information available on the internet. The database presently contains 39226 titles. Journal information includes the description (aims and scope), journal abbreviation, journal homepage link, subject category and ISSN.

Current Contents - Clinical Medicine Current Contents - Clinical Medicine provides easy access to complete tables of contents, abstracts, bibliographic information and all other significant items in recently published issues from over 1,000 leading journals in clinical medicine.

BIOSIS Previews BIOSIS Previews is an English-language, bibliographic database service, with abstracts and citation indexing. It is part of Clarivate Analytics Web of Science suite. BIOSIS Previews indexes data from 1926 to the present.

Journal Citation Reports/Science Edition Journal Citation Reports/Science Edition aims to evaluate a journal’s value from multiple perspectives including the journal impact factor, descriptive data about a journal’s open access content as well as contributing authors, and provide readers a transparent and publisher-neutral data & statistics information about the journal.

Submission Turnaround Time

Conferences

Top