Presence of 17 beta-hydroxysteroid dehydrogenase type 3 messenger ribonucleic acid transcript in an ovarian Sertoli-Leydig cell tumor

Fertil Steril. 1997 Sep;68(3):534-7. doi: 10.1016/s0015-0282(97)00233-1.

Abstract

Objective: To evaluate the level of 17 beta-hydroxysteroid dehydrogenase (17 beta-HSD) type 1, 2, and 3 transcripts in a Sertoli-Leydig cell tumor, adjacent theca lutein ovarian tissue, and normal control ovarian stromal tissue.

Setting: An academic medical center.

Design: Total RNA was extracted from formalin-fixed, paraffin-embedded tissue slides and used for reverse transcription-polymerase chain reaction (RT-PCR) with primers specific for 17 beta-HSD types 1, 2, or 3. The PCR products were subjected to Southern hybridization with 5' [32P] end-labeled internal primers for each type of the isozymes.

Patient(s): A 35-year-old woman with a Sertoli-Leydig cell tumor on her right ovary. The tumor and the right ovary were surgically removed. Control ovarian stromal tissue was obtained from a woman undergoing hysterectomy for uterine leiomyomata.

Result(s): In the control ovarian stromal tissue, the transcripts for the type 1 and type 2 isoforms were the predominant transcripts detected. In the Sertoli-Leydig cell tumor, the transcript for the type 3 isoform was the predominant transcript detected. Ovarian tissue from the same ovary as the Sertoli-Leydig cell tumor (diagnosed as theca lutein cysts on histologic examination) expressed the type 2 and 3 transcripts.

Conclusion(s): The 17 beta-HSD type 3 isoform efficiently converts androstenedione to T and is the predominant HSD isoform in the testis. In hyperandrogenism caused by a Sertoli-Leydig cell tumor, both the tumor tissue and nontumor tissue from the same ovary expressed the "testicular" form of the 17 beta-HSD.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 17-Hydroxysteroid Dehydrogenases / genetics*
  • Adult
  • Female
  • Humans
  • Isoenzymes / genetics*
  • Ovarian Neoplasms / enzymology*
  • RNA, Messenger / analysis*
  • Sertoli-Leydig Cell Tumor / enzymology*

Substances

  • Isoenzymes
  • RNA, Messenger
  • 17-Hydroxysteroid Dehydrogenases