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Prostate cell lines as models for biomarker discovery: Performance of current markers and the search for new biomarkers

机译:前列腺细胞系作为生物标志物发现的模型:当前标志物的性能和寻找新的生物标志物

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Prostate cancer cell lines have been used in the search for biomarkers that are suitable for prostate cancer diagnosis. Unfortunately, many cell line studies have only involved single cell lines, partially characterized cell lines or were performed without controls, and this may have been detrimental to effective biomarker discovery. We have analyzed a panel of prostate cancer and nonmalignant control cell lines using current biomarkers and then investigated a set of prospective endosomal and lysosomal proteins to search for new biomarkers. METHODS Western blotting was used to define the amount of protein and specific molecular forms in cell extracts and culture media from a panel of nonmalignant (RWPE-1, PNT1a, PNT2) and prostate cancer (22RV1, CaHPV10, DU-145, LNCaP) cell lines. Gene expression was determined by qRT-PCR. RESULTS HPV-18 transfected cell lines displayed a different pattern of protein and gene expression when compared to the other cell lines examined, suggesting that these cell lines may not be the most optimal for prostate cancer biomarker discovery. There was an increased amount of prostatic acid phosphatase and kallikrein proteins in LNCaP cell extracts and culture media, but variable amounts of these proteins in other prostate cancer cell lines. There were minimal differences in the amounts of lysosomal proteins detected in prostate cancer cells and culture media, but two endosomal proteins, cathepsin B and acid ceramidase, had increased gene and protein expression, and certain molecular forms showed increased secretion from prostate cancer cells (P ≤ 0.05). LIMP-2 gene and protein expression was significantly increased in prostate cancer compared to nonmalignant cell lines (P ≤ 0.05). CONCLUSIONS While the existing prostate cancer biomarkers and lysosomal proteins investigated here were not able to specifically differentiate between a panel of nonmalignant and prostate cancer cell lines, endosomal proteins showed some discriminatory capacity. LIMP-2 is a critical regulator of endosome biogenesis and the increased expression observed in prostate cancer cells indicated that other endosome related proteins may also be upregulated and could be investigated as novel biomarkers. Prostate 74:547-560, 2014.
机译:前列腺癌细胞系已用于寻找适合前列腺癌诊断的生物标志物。不幸的是,许多细胞系研究仅涉及单个细胞系,部分表征的细胞系或在没有对照的情况下进行,这可能对有效的生物标记物发现有害。我们已经使用当前的生物标记物分析了一组前列腺癌和非恶性对照细胞系,然后研究了一组预期的内体和溶酶体蛋白以寻找新的生物标记物。方法采用蛋白质印迹法确定一组非恶性(RWPE-1,PNT1a,PNT2)和前列腺癌(22RV1,CaHPV10,DU-145,LNCaP)细胞的细胞提取物和培养基中蛋白质和特定分子形式的数量线。通过qRT-PCR确定基因表达。结果与检测的其他细胞系相比,HPV-18转染的细胞系显示出不同的蛋白质和基因表达模式,表明这些细胞系可能不是最适合发现前列腺癌生物标志物的细胞系。 LNCaP细胞提取物和培养基中前列腺酸磷酸酶和激肽释放酶蛋白的含量增加,而在其他前列腺癌细胞系中这些蛋白的含量却有所变化。在前列腺癌细胞和培养基中检测到的溶酶体蛋白含量差异很小,但是两种内体蛋白,组织蛋白酶B和酸性神经酰胺酶,具有增加的基因和蛋白表达,并且某些分子形式显示出前列腺癌细胞的分泌增加(P ≤0.05)。与非恶性细胞系相比,前列腺癌中的LIMP-2基因和蛋白质表达显着增加(P≤0.05)。结论虽然此处研究的现有前列腺癌生物标志物和溶酶体蛋白不能特异性区分一组非恶性和前列腺癌细胞系,但内体蛋白显示出一定的区分能力。 LIMP-2是内体生物发生的关键调节剂,在前列腺癌细胞中观察到的表达增加表明其他内体相关蛋白也可能被上调,可以作为新型生物标记物进行研究。前列腺74:547-560,2014年。

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