Article Data

  • Views 500
  • Dowloads 128

Original Research

Open Access

Expression levels of C19MC and C14MC microRNAs in complete hydatidiform moles and ovarian mature cystic teratomas

  • K. Miura1,*,
  • Y. Hasegawa1
  • M.Yamada1
  • A. Higashijima1
  • S. Miura1
  • M. Kaneuchi1
  • H. Masuzaki1

1Department of Obstetrics and Gynecology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki (Japan)

DOI: 10.12892/ejgo4014.2018 Vol.39,Issue 2,April 2018 pp.277-280

Published: 10 April 2018

*Corresponding Author(s): K. Miura E-mail: docjwxf@126.com

Abstract

Aim: To investigate whether comparative analysis of microRNA (miR) expression patterns in complete hydatidiform moles (androgenic origin) and ovarian mature cystic teratomas (parthenogenetic origin) could form the basis of a systematic screening system for parental allele-specific miRs, we measured expression in these tissues of the chromosome 19 miR cluster (C19MC; miR-517a, miR517c, and miR-518b), which has a paternal allele-specific expression pattern, and of C14MC (miR-323-3p), which also has a maternal allele-specific expression pattern. Materials and Methods: Sixteen cases of complete hydatidiform mole and 11 cases of ovarian teratoma were studied. Expression of each miR was measured by real-time quantitative reverse transcription-polymerase chain reaction, and the expression levels were compared in copies/mL. Statistical significance was defined as p < 0.05 by the Mann–Whitney non-parametric U test. Results: The median and (range) expression levels of miR-517a, -517c, and -518b in the hydatidiform moles were 747,082.6 (5,075.7–4,701,041.6), 480,759.6 (3,436.5–2,053,419.8), and 192,930.1 (37,478.7–4,381,175.2) copies/mL, respectively. Conversely, their expression levels in ovarian teratomas were below the limit of detection. The expression level of miR-323-3p was significantly higher in the ovarian teratomas at 9,700.7 (1,663.8–144,248.0) copies/mL than in the hydatidiform moles at 1,665.1 (193.4–5,029.5) copies/mL (p = 0.02). Conclusions: C19MC miRs were detected only in androgenic tissues. The C14MC miR-323-3p was detected in both types but it was significantly higher in parthenogenetic than in androgenic tissues. Thus, comparative analysis of miR expression patterns between these tissue types will help in developing a screening system for parental-specific miRs.

Keywords

Androgenic; C19MC; C14MC; Hydatidiform mole; Ovarian teratoma; Parthenogenetic; Parental allele-specific expression.

Cite and Share

K. Miura,Y. Hasegawa,M.Yamada,A. Higashijima,S. Miura,M. Kaneuchi,H. Masuzaki. Expression levels of C19MC and C14MC microRNAs in complete hydatidiform moles and ovarian mature cystic teratomas. European Journal of Gynaecological Oncology. 2018. 39(2);277-280.

References

[1] Chim S.S., Shing T.K., Hung E.C., Leung T.Y., Lau T.K., Chiu R.W., et al.: “Detection and characterization of placental microRNAs in maternal plasma”. Clin. Chem., 2008, 54, 482.

[2] Miura K., Miura S., Yamasaki K., Higashijima A., Kinoshita A., Yoshiura K., et al.: “Identification of pregnancy-associated microRNAs in maternal plasma”. Clin. Chem., 2010, 56, 1767.

[3] Noguer-Dance M., Abu-Amero S., Al-Khtib M., Lefèvre A., Coullin P., Moore G.E., et al.: “The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta”. Hum. Mol. Genet., 2010, 19, 3566.

[4] Morales-Prieto D.M., Ospina-Prieto S., Chaiwangyen W., Schoenleben M., Markert U.R..: “Pregnancy-associated miRNA-clusters”. J. Reprod. Immunol., 2013, 97, 51.

[5] Ohama K., Kajii T., Okamoto E., Fukuda Y., Imaizumi K., Tsukahara M., et al.: “Dispermic origin of XY hydatidiform moles”. Nature, 1981, 292, 551.

[6] Miura K., Obama M., Yun K., Masuzaki H., Ikeda Y., Yoshimura S., et al.: “Methylation imprinting of H19 and SNRPN genes in human benign ovarian teratomas”. Am. J. Hum. Genet., 1999, 65, 1359.

[7] Higashijima A., Miura K., Mishima H., Kinoshita A., Jo O., Abe S., et al.: “ Characterization of placenta-specific microRNAs in fetal growth restriction pregnancy”. Prenat. Diagn., 2013, 33, 214.

[8] Miura K., Miyoshi O., Yun K., Inazawa J., Miyamoto T., Hayashi H., et al.: “Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta”. J. Hum. Genet., 1999, 44, 1.

[9] Peters J., Robson J.E., “Imprinted noncoding RNAs”. Mamm. Genome, 2008, 19, 493.

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