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小鼠正常及前列腺上皮内瘤变发展过程中生长分化因子15的表达动态

Dynamics of expression of growth differentiation factor 15 in normal and PIN development in the mouse.

作者信息

Noorali Samina, Kurita Takeshi, Woolcock Bruce, de Algara Teresa Ruiz, Lo Maisie, Paralkar Vishwas, Hoodless Pamela, Vielkind Juergen

机构信息

Department of Cancer Endocrinology, BC Cancer Research Centre/BC Cancer Agency, Vancouver, BC, Canada.

出版信息

Differentiation. 2007 Apr;75(4):325-36. doi: 10.1111/j.1432-0436.2006.00142.x. Epub 2007 Feb 5.

Abstract

Growth differentiation factor (GDF15) is a distant member of the transforming growth factor-beta superfamily, a diverse group of structurally related proteins that exert multiple effects on cell fate such as on cell growth and differentiation but little is known about GDF15 in these processes. Previously we observed the mature GDF15 to be associated with human prostate carcinogenesis hence prompting us to study GDF15 further. Here we report gdf15 expression both at the RNA and protein levels, in normal prostatic tissues of wild type (wt) and prostatic intraepithelial neoplasia (PIN) of transgenic (Tg) 12T-7s model mice during embryonic, postnatal, and adult prostate formation up to 15 weeks after birth. Dynamic changes in expression, at both the mRNA and protein level, correlated with cell proliferation and differentiation during distinct phases of normal mouse prostate development and alterations in the dynamics of gdf15 expression correlated with the changes in development resulting in PIN formation. Most notably mature gdf15 protein was significantly elevated during hyperplasia and PIN development. Changes in the protein levels did not always correlate well with the mRNA levels. This was more prominent during PIN than during normal prostate development suggesting that this may also be an indicator of disturbed regulation of gdf15 in PIN. We propose that gdf15 is a growth factor with dual function either promoting proliferation or growth arrest and differentiation due most likely to differences in cellular differentiation. Because of the differentiation defect in PIN its epithelium no longer responds to gdf15 by cellular growth arrest as does the normal epithelium and gdf may even stimulate proliferation. The data supports our hypothesis that GDF15 plays a role in the early stages of human prostate cancer.

摘要

生长分化因子(GDF15)是转化生长因子-β超家族的一个远亲成员,该超家族由一组结构相关的蛋白质组成,它们对细胞命运有多种影响,如细胞生长和分化,但人们对GDF15在这些过程中的了解甚少。此前我们观察到成熟的GDF15与人类前列腺癌发生有关,因此促使我们进一步研究GDF15。在此我们报告了在野生型(wt)正常前列腺组织以及转基因(Tg)12T - 7s模型小鼠的前列腺上皮内瘤变(PIN)中,从胚胎期、出生后到出生后15周成年前列腺形成过程中GDF15在RNA和蛋白质水平的表达情况。在正常小鼠前列腺发育的不同阶段,mRNA和蛋白质水平的表达动态变化与细胞增殖和分化相关,而GDF15表达动态的改变与导致PIN形成的发育变化相关。最显著的是,成熟的GDF15蛋白在增生和PIN发展过程中显著升高。蛋白质水平的变化并不总是与mRNA水平良好相关。这在PIN期间比在正常前列腺发育期间更为突出,表明这也可能是PIN中GDF15调节紊乱的一个指标。我们提出GDF15是一种具有双重功能的生长因子,根据细胞分化的差异,它可能促进增殖或生长停滞及分化。由于PIN中的分化缺陷,其上皮不再像正常上皮那样通过细胞生长停滞对GDF15作出反应,GDF甚至可能刺激增殖。这些数据支持了我们的假设,即GDF15在人类前列腺癌的早期阶段发挥作用。

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