microvascular density

微血管密度
  • 文章类型: Journal Article
    MCAM-1(CD146)是属于免疫球蛋白超家族的内皮细胞粘附分子。最近的研究已经确定CD146表达是肿瘤进展的关键标志物。迁移,和各种恶性肿瘤的转移。本研究旨在评估CD146在各种妇科肿瘤中的免疫组织化学表达。
    这项研究是在印度中部的三级医疗中心进行的。共包括49例妇科癌症病例和16个部位匹配的对照。病例包括27例宫颈,10子宫内膜,10卵巢,和两种杂项癌症。进行CD146免疫组织化学并评估免疫反应性评分(IRS),微血管密度(MVD),和微血管口径(MVC)。5或更多的IRS被认为是CD146阳性。
    病例与CD146阳性的p值宫颈对照组分别为0.0531、0.0580和0.007,子宫内膜,和卵巢部位,分别。与良性组织相比,病例的平均MVD明显更高(p值<0.00001),与对照组相比,病例的平均MVC较小(p值<0.0001)。
    在妇科恶性肿瘤中发现CD146的MVD较高,强调其在癌症新血管生成中的作用及其潜在的治疗作用。CD146上皮表达在卵巢癌中也显著增高。需要进行更大样本量的进一步研究,以确认该蛋白质可能是妇科癌症的潜在神学靶标。
    UNASSIGNED: MCAM-1 (CD146) is an endothelial cell adhesion molecule belonging to the immunoglobulin superfamily. Recent studies have identified CD146 expression as a critical marker for tumor progression, migration, and metastasis in various malignancies. This study aimed to evaluate CD146 immunohistochemical expression in various gynecological cancers.
    UNASSIGNED: This study was conducted in a tertiary medical center in central India. A total of 49 gynecological cancer cases and 16 site-matched controls were included. The cases comprised 27 cervical, 10 endometrial, 10 ovarian, and two miscellaneous cancers. CD146 immunohistochemistry was performed and assessed for immunoreactivity score (IRS), microvascular density (MVD), and microvascular caliber (MVC). An IRS of 5 or more was considered CD146 positive.
    UNASSIGNED: The p-values for CD146 positivity for cases vs. control were 0.0531, 0.0580, and 0.007 for cervical, endometrial, and ovarian sites, respectively. The mean MVD was found to be significantly higher in cases compared with benign tissues (p-value <0.00001), and the mean MVC of cases was found to be smaller when compared with the controls (p-value <0.0001).
    UNASSIGNED: MVD by CD146 was found to be higher in gynecological malignancies, highlighting its role in cancer neo-angiogenesis and its potential therapeutic role. CD146 epithelial expression was also significantly higher in ovarian cancers. Further studies with a larger sample size are required to confirm that this protein may be a potential theognostic target in gynecological cancers.
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