4.5 Article

Prolactin is Expressed in Uterine Leiomyomas and Promotes Signaling and Fibrosis in Myometrial Cells

Journal

REPRODUCTIVE SCIENCES
Volume 29, Issue 9, Pages 2525-2535

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s43032-021-00741-w

Keywords

Leiomyoma; Myometrium; Prolactin; Prolactin receptor; Dopamine D2 receptor

Funding

  1. NIH [R01CA193583, T32AI007285]
  2. Richard W. and Mae Stone Goode Grant Program

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Uterine leiomyomas are benign tumors that are sensitive to estrogen and influenced by other hormones like prolactin. The presence of prolactin-producing cells in leiomyomas suggests a potential role in promoting fibrotic growth. Prolactin activates signaling pathways and myofibroblast markers in myometrial cells, contributing to the understanding of the development of leiomyomas.
Uterine leiomyomas are benign, estrogen-sensitive, fibrotic smooth muscle cell tumors occurring in the uterine myometrium. Leiomyomas are a considerable health burden, with a lifetime prevalence of 80% and limited treatment options. Estrogen and progesterone have positive effects on leiomyoma growth, but little is known about the roles of other hormones. One hormone of interest is prolactin, as it has been described to be present and functional in leiomyomas. The current study investigates prolactin production within leiomyomas and its effects on myometrial cells. RNA isolation and quantitative-PCR of human leiomyoma samples relative to matched adjacent myometrium confirms significant expression of prolactin and dopamine receptor D2, a known regulator of prolactin production and release in the pituitary, with no difference in prolactin receptor expression. Immunohistochemistry confirms increased prolactin in leiomyomas compared to adjacent myometrium and uteri from women without leiomyomas. These results suggest that leiomyomas contain cells that produce prolactin, which may then promote signaling in leiomyoma cells to regulate leiomyoma development/growth. Accordingly, we find that prolactin robustly activates STAT5 and MAPK signaling in rat and human myometrial cell lines. Furthermore, prolactin stimulates expression of myofibroblast markers in rat myometrial cells. Our findings suggest that local prolactin production in leiomyomas may stimulate trans-differentiation of myometrial cells to myofibroblasts, which in turn contributes to the fibrotic nature of leiomyomas.

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