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蛋白酶M在卵巢肿瘤中的表达增加。

Increased expression of protease M in ovarian tumors.

作者信息

Tanimoto H, Underwood L J, Shigemasa K, Parmley T H, O'Brien T J

机构信息

Department of Obstetrics and Gynecology, Asada General Hospital, Marugame, Kagawa, Japan.

出版信息

Tumour Biol. 2001 Jan-Feb;22(1):11-8. doi: 10.1159/000030150.

Abstract

Proteases are known to play important roles in tumor invasion and metastasis. Protease M, which was originally identified by Anisowicz and colleagues in 1996, is a new member of the serine protease family. We also identified the protease M transcript in a differential PCR screen of ovarian tumors and have investigated its expression in 44 ovarian tumors (12 low malignant potential tumors, 32 carcinomas) and 10 normal ovaries using quantitative PCR. The PCR product was labeled with (32)P and a phosphoimager was used to determine the relative expression of the protease M gene compared to internal control beta-tubulin. mRNA expression levels of protease M were significantly elevated in 9 of 12 low malignant potential tumors and 30 of 32 carcinomas. Northern blot hybridization showed that the 1.7-kb protease M transcript was abundant in carcinoma but not detected in normal ovary. Immunohistochemical staining of normal ovary and ovarian tumor tissue sections with antibodies generated to protease M derived peptides corroborated the semi-quantitative PCR and Northern analysis data. Our results suggest that protease M is frequently overexpressed in ovarian tumors and may therefore contribute to the invasive nature or growth capacity of ovarian carcinomas.

摘要

已知蛋白酶在肿瘤侵袭和转移中发挥重要作用。蛋白酶M最初由阿尼索维茨及其同事于1996年鉴定,是丝氨酸蛋白酶家族的新成员。我们还在卵巢肿瘤的差异PCR筛选中鉴定出蛋白酶M转录本,并使用定量PCR研究了其在44例卵巢肿瘤(12例低恶性潜能肿瘤、32例癌)和10例正常卵巢中的表达。PCR产物用(32)P标记,并用磷成像仪测定蛋白酶M基因相对于内对照β-微管蛋白的相对表达。蛋白酶M的mRNA表达水平在12例低恶性潜能肿瘤中的9例以及32例癌中的30例显著升高。Northern印迹杂交显示,1.7kb的蛋白酶M转录本在癌组织中丰富,但在正常卵巢中未检测到。用针对蛋白酶M衍生肽产生的抗体对正常卵巢和卵巢肿瘤组织切片进行免疫组织化学染色,证实了半定量PCR和Northern分析数据。我们的结果表明,蛋白酶M在卵巢肿瘤中经常过度表达,因此可能有助于卵巢癌的侵袭性或生长能力。

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