Download e-book for kindle: Endocrine Oncology (Contemporary Endocrinology) by Stephen P. Ethier

By Stephen P. Ethier

ISBN-10: 0896036219

ISBN-13: 9780896036215

ISBN-10: 1592592236

ISBN-13: 9781592592234

Stephen P. Ethier and a panel of major investigators comprehensively study the mobile, molecular, and endocrine components within the improvement of cancers of the breast, prostate, endometrium, and ovary. focusing on defining crucial unresolved concerns within the box, the authors overview how steroid hormones functionality to control common mammary gland homeostasis in people, with specific emphasis at the roles of estrogen, progesterone, and progress components. complete and updated, Endocrine Oncology bargains either simple and scientific researchers not just the most recent molecular and mobile findings on endocrine cancers, but additionally a strong serious research that may end up useful to all endocrinologists and oncologists operating within the quarter at the present time.

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Extra resources for Endocrine Oncology (Contemporary Endocrinology)

Example text

Using a semiquantitative RT-triple primer PCR approach (26), which simultaneously measures the relative expression of the WT hER`1 and the two variant hER`2 and hER`5 mRNAs, it appears that, in most, but not all, cases, the level of the variant mRNA species exceeds that of the WT hER`1 (Fig. 5; unpublished data) in both normal and neoplastic human breast tissues. The known sequence of all human ER`-like transcripts is shown schematically in Fig. 6; also shown in this figure are the proteins predicted to be encoded by these variant hER` mRNAs.

These same authors reported a trend toward higher relative expression of exon-5-deleted ER_ mRNA in primary tumors of women who relapsed, compared to primary tumors of those that did not relapse. Together, these data suggest that, in addition to altered expression of ER_ variant mRNA, which occurs during breast tumorigenesis, further changes in ER_ variant expression may occur during BC progression. However, another study (34) has recently found no significant differences in the relative expression of clone-4truncated, exon-5-deleted, and exon-7-deleted ER_ mRNAs, between a series of primary breast tumors and their matched concurrent lymph node metastasis, suggesting that altered expression of ER_ variant mRNAs probably occurs prior to the acquisition of the ability to metastasize, and therefore may be a marker of future metastatic potential.

Preliminary data suggests that this is also true for samples of ER-positive breast tumors and their matched, adjacent normal tissues (29a); there is also evidence suggesting that an exon3-deleted ER_ variant mRNA is decreased in BCs, compared to normal human breast epithelium (29). Because this ER_ variant mRNA encodes a protein that can inhibit WT ER_ transcriptional activity (30) and causes growth suppression when stably overexpressed in ER-positive MCF-7 human BC cells (29), it was concluded that the exon3-deleted ER_ variant may function to attenuate estrogenic effects in normal mammary epithelium.

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Endocrine Oncology (Contemporary Endocrinology) by Stephen P. Ethier


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