Prolactin receptor gene transcriptional control, regulatory modalities relevant to breast cancer resistance and invasiveness
The prolactin receptor (PRLR) is a member of the lactogen/cytokine receptor family, which mediates multiple actions of prolactin (PRL). PRL is a major hormone in the proliferation/differentiation of breast epithelium that is essential for lactation. It is also involved in breast cancer development,...
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| Format: | Article |
| Language: | English |
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Frontiers Media S.A.
2022-09-01
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| Series: | Frontiers in Endocrinology |
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| Online Access: | https://www.frontiersin.org/articles/10.3389/fendo.2022.949396/full |
| _version_ | 1797995352000823296 |
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| author | Raghuveer Kavarthapu Maria L. Dufau |
| author_facet | Raghuveer Kavarthapu Maria L. Dufau |
| author_sort | Raghuveer Kavarthapu |
| collection | DOAJ |
| description | The prolactin receptor (PRLR) is a member of the lactogen/cytokine receptor family, which mediates multiple actions of prolactin (PRL). PRL is a major hormone in the proliferation/differentiation of breast epithelium that is essential for lactation. It is also involved in breast cancer development, tumor growth and chemoresistance. Human PRLR expression is controlled at the transcriptional level by multiple promoters. Each promoter directs transcription/expression of a specific non-coding exon 1, a common non-coding exon 2 and coding exons E3-11. The identification of exon 11 of PRLR led to finding of alternative spliced products and two novel short forms (SF) that can inhibit the long form (LF) of PRLR activity with relevance in physiological regulation and breast cancer. Homo and heterodimers of LF and SF are formed in the absence of PRL that acts as a conformational modifier. Heterodimerization of SF with LF is a major mechanism through which SF inhibits some signaling pathways originating at the LF. Biochemical/molecular modeling approaches demonstrated that the human PRLR conformation stabilized by extracellular intramolecular S−S bonds and several amino acids in the extracellular D1 domain of PRLR SF are required for its inhibitory actions on PRLR LF-mediated functions. Studies in breast cancer cells demonstrated that the transcription of PRLR was directed by the preferentially utilized PIII promoter, which lacks an estrogen responsive element. Complex formation of non-DNA bound ERα dimer with Sp1 and C/EBPβ dimers bound to their sites at the PRLR promoter is required for basal activity. Estradiol induces transcriptional activation/expression of the PRLR gene, and subsequent studies revealed the essential role of autocrine PRL released by breast cancer cells and CDK7 in estradiol-induced PRLR promoter activation and upregulation. Other studies revealed stimulation of the PRLR promoter activity and PRLR LF protein by PRL in the absence of estrogen via the STAT5/phospho-ERα activation loop. Additionally, EGF/ERBB1 can induce the transcription of PRLR independent of estrogen and prolactin. The various regulatory modalities contributing to the upregulation of PRLR provide options for the development of therapeutic approaches to mitigate its participation in breast cancer progression and resistance. |
| first_indexed | 2024-04-11T10:00:14Z |
| format | Article |
| id | doaj.art-1530c508f8a84ce5a6d0d7c9e13280af |
| institution | Directory Open Access Journal |
| issn | 1664-2392 |
| language | English |
| last_indexed | 2024-04-11T10:00:14Z |
| publishDate | 2022-09-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Endocrinology |
| spelling | doaj.art-1530c508f8a84ce5a6d0d7c9e13280af2022-12-22T04:30:27ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922022-09-011310.3389/fendo.2022.949396949396Prolactin receptor gene transcriptional control, regulatory modalities relevant to breast cancer resistance and invasivenessRaghuveer KavarthapuMaria L. DufauThe prolactin receptor (PRLR) is a member of the lactogen/cytokine receptor family, which mediates multiple actions of prolactin (PRL). PRL is a major hormone in the proliferation/differentiation of breast epithelium that is essential for lactation. It is also involved in breast cancer development, tumor growth and chemoresistance. Human PRLR expression is controlled at the transcriptional level by multiple promoters. Each promoter directs transcription/expression of a specific non-coding exon 1, a common non-coding exon 2 and coding exons E3-11. The identification of exon 11 of PRLR led to finding of alternative spliced products and two novel short forms (SF) that can inhibit the long form (LF) of PRLR activity with relevance in physiological regulation and breast cancer. Homo and heterodimers of LF and SF are formed in the absence of PRL that acts as a conformational modifier. Heterodimerization of SF with LF is a major mechanism through which SF inhibits some signaling pathways originating at the LF. Biochemical/molecular modeling approaches demonstrated that the human PRLR conformation stabilized by extracellular intramolecular S−S bonds and several amino acids in the extracellular D1 domain of PRLR SF are required for its inhibitory actions on PRLR LF-mediated functions. Studies in breast cancer cells demonstrated that the transcription of PRLR was directed by the preferentially utilized PIII promoter, which lacks an estrogen responsive element. Complex formation of non-DNA bound ERα dimer with Sp1 and C/EBPβ dimers bound to their sites at the PRLR promoter is required for basal activity. Estradiol induces transcriptional activation/expression of the PRLR gene, and subsequent studies revealed the essential role of autocrine PRL released by breast cancer cells and CDK7 in estradiol-induced PRLR promoter activation and upregulation. Other studies revealed stimulation of the PRLR promoter activity and PRLR LF protein by PRL in the absence of estrogen via the STAT5/phospho-ERα activation loop. Additionally, EGF/ERBB1 can induce the transcription of PRLR independent of estrogen and prolactin. The various regulatory modalities contributing to the upregulation of PRLR provide options for the development of therapeutic approaches to mitigate its participation in breast cancer progression and resistance.https://www.frontiersin.org/articles/10.3389/fendo.2022.949396/fullprolactin receptor (PRLR)transcriptional regulationgene structuresignal transductionbreast cancerprolactin (PRL) |
| spellingShingle | Raghuveer Kavarthapu Maria L. Dufau Prolactin receptor gene transcriptional control, regulatory modalities relevant to breast cancer resistance and invasiveness Frontiers in Endocrinology prolactin receptor (PRLR) transcriptional regulation gene structure signal transduction breast cancer prolactin (PRL) |
| title | Prolactin receptor gene transcriptional control, regulatory modalities relevant to breast cancer resistance and invasiveness |
| title_full | Prolactin receptor gene transcriptional control, regulatory modalities relevant to breast cancer resistance and invasiveness |
| title_fullStr | Prolactin receptor gene transcriptional control, regulatory modalities relevant to breast cancer resistance and invasiveness |
| title_full_unstemmed | Prolactin receptor gene transcriptional control, regulatory modalities relevant to breast cancer resistance and invasiveness |
| title_short | Prolactin receptor gene transcriptional control, regulatory modalities relevant to breast cancer resistance and invasiveness |
| title_sort | prolactin receptor gene transcriptional control regulatory modalities relevant to breast cancer resistance and invasiveness |
| topic | prolactin receptor (PRLR) transcriptional regulation gene structure signal transduction breast cancer prolactin (PRL) |
| url | https://www.frontiersin.org/articles/10.3389/fendo.2022.949396/full |
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