首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Expression of mRNAs for type I and type III procollagens in serous ovarian cystadenomas and cystadenocarcinomas.
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Expression of mRNAs for type I and type III procollagens in serous ovarian cystadenomas and cystadenocarcinomas.

机译:浆液性卵巢囊腺瘤和囊腺癌中I型和III型前胶原mRNA的表达。

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摘要

Malignant ovarian tumors induce a strong fibro-proliferative reaction characterized by the active production of type I and type III procollagen both locally in the ovary as well as more remotely in the peritoneal cavity. Our purpose was to determine the origin of the increased collagen production observed in serous ovarian tumors with different histological grades of malignancy, ie, whether the malignant cells or the stromal fibroblasts are responsible for the synthesis of collagen fibers. We visualized the mRNAs corresponding to the pro alpha 1(I) and pro alpha 2(I) chains of type I procollagen and the pro alpha 1(III) chain of type III procollagen by in situ hybridization. Strong signals for both chains of type I procollagen were seen in stromal fibroblasts next to tumor cell islets, whereas the reaction was weak or absent near benign ovarian cysts. In poorly differentiated tumors, the signals were particularly abundant and occasionally also seen in the neoplastic cells themselves. Type III procollagen mRNA expression was similar, although somewhat less distinct. These findings indicate that the production of interstitial procollagens is related to the degree of malignancy and neoplastic activity of tumors. The formation of collagen in well differentiated ovarian tumors is a function of stromal fibroblasts, whereas in poorly differentiated tumors, aberrant expression of one or several chains of type I and type III procollagens in the neoplastic cells is also likely to take place.
机译:恶性卵巢肿瘤会诱导强烈的纤维增生反应,其特征是在卵巢内以及腹膜腔内均会主动产生I型和III型胶原蛋白。我们的目的是确定在具有不同组织学级别恶性程度的浆液性卵巢肿瘤中观察到的胶原蛋白产生增加的起源,即,恶性细胞或基质成纤维细胞是胶原蛋白纤维合成的原因。我们通过原位杂交可视化了对应于I型胶原蛋白的亲α1(I)和pro alpha 2(I)链和III型胶原蛋白的亲α1(III)链的mRNA。在肿瘤细胞胰岛旁的间质成纤维细胞中观察到了两条I型胶原蛋白原链的强信号,而该反应在卵巢良性囊肿附近微弱或不存在。在低分化的肿瘤中,信号特别丰富,有时在肿瘤细胞本身中也能看到。 III型前胶原mRNA的表达相似,尽管区别不大。这些发现表明,间质前胶原的产生与肿瘤的恶性程度和肿瘤活性有关。高分化卵巢肿瘤中胶原蛋白的形成是间质成纤维细胞的功能,而在低分化肿瘤中,I型和III型前胶原的一条或几条链也可能在肿瘤细胞中异常表达。

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