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Clin Trans Gastroenterology: 前列腺特异性膜抗原在肿瘤相关血管系统中的表达可以预测肝细胞癌预后不良

2019-06-26 不详 MedSci原创

前列腺特异性膜抗原(PSMA)最初是被发现在正常前列腺中特异性表达,其表达水平在前列腺癌的几乎所有阶段都被上调。近年来,还发现PSMA在许多非前列腺实体瘤中与肿瘤相关的脉管系统中表达。然而,PSMA在肝细胞癌(HCC)中的表达模式尚未得到很好的研究。因此,本项研究旨在探究二者的关系。

背景及目的:
前列腺特异性膜抗原(PSMA)最初是被发现在正常前列腺中特异性表达,其表达水平在前列腺癌的几乎所有阶段都被上调。近年来,还发现PSMA在许多非前列腺实体瘤中与肿瘤相关的脉管系统中表达。然而,PSMA在肝细胞癌(HCC)中的表达模式尚未得到很好的研究。因此,本项研究旨在探究二者的关系。

方法:
在本研究中,研究人员使用免疫组织化学染色检测了103例HCC组织中PSMA的表达水平,并分析了PSMA表达与其他临床病理特征和预后之间的关系。

结果:
103例患者中,27例(26%)在超过50%的肿瘤相关血管中显示PSMA表达上调,49例(48%)显示PSMA表达少于50%的脉管系统,27例(26%) )没有可检测到的PSMA表达。血管PSMA表达与几种临床病理特征相关,如肿瘤分期,肿瘤分化,淋巴结转移和Ki-67指数。此外,高血管PSMA表达也与HCC患者预后不良有关。单变量和多变量分析显示高血管PSMA表达可用作HCC的独立预后标志物。

讨论:
PSMA在HCC的肿瘤相关脉管系统中特异性表达,并且血管PSMA表达可以用作HCC的新型预后标志物和血管治疗新型生物标志物。

原始出处:

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    2020-03-03 bsmagic9140
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  5. 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  6. 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  7. 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status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1504709, encodeId=817f1504e0914, content=<a href='/topic/show?id=7730e85412' target=_blank style='color:#2F92EE;'>#Gastroenterology#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=58, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=7854, encryptionId=7730e85412, topicName=Gastroenterology)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=5fc29706655, createdName=chaojitidian, createdTime=Fri Jun 28 08:00:00 CST 2019, time=2019-06-28, status=1, ipAttribution=)]
    2020-02-28 许安
  8. 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status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1504709, encodeId=817f1504e0914, content=<a href='/topic/show?id=7730e85412' target=_blank style='color:#2F92EE;'>#Gastroenterology#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=58, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=7854, encryptionId=7730e85412, topicName=Gastroenterology)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=5fc29706655, createdName=chaojitidian, createdTime=Fri Jun 28 08:00:00 CST 2019, time=2019-06-28, status=1, ipAttribution=)]
    2019-10-12 xjy02
  9. 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