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首页> 外文期刊>Clinical and Experimental Metastasis >Profiling immunohistochemical expression of NOTCH1–3, JAGGED1, cMET, and phospho-MAPK in 100 carcinomas of unknown primary
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Profiling immunohistochemical expression of NOTCH1–3, JAGGED1, cMET, and phospho-MAPK in 100 carcinomas of unknown primary

机译:NOTCH1-3,JAGGED1,cMET和磷酸化MAPK在100例原发性未知癌中的免疫组化表达分析

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Cancer of unknown primary (CUP) is a heterogeneous entity, managed on the basis of “one size fits all” therapeutic concepts; insights into the molecular biology of CUP are urgently needed. We retrospectively examined the immunohistochemical (IHC) expression of Notch1, 2, 3, Jagged1, cMET, and pMAPK biomolecules in 100 CUP tumors using tissue microarrays, aiming to study their correlation to clinicopathologic characteristics and prognostic utility for patient outcome. Notch3 and pMAPK were most frequently expressed (97 and 91 %, respectively). A linear correlation of Notch3 and cMET expression was found (p = 0.001), while pMAPK emerged as the major adverse prognostic factor (median overall survival OS 9 vs. 17 months, p = 0.016), carrying also a significantly positive predictive value (p = 0.02). Our study indicated a favorable prognostic impact of cMET expression in CUP, both in univariate (median OS 15 vs. 9 months, p = 0.05) and in multivariate analysis (Relative Risk RR for death 0.48, p = 0.025). cMET and Notch3 expression were found to be statistically more frequent in squamous carcinomas (positive in 90 % of cases), associated with a unique metastatic IHC pattern (cMET-high in soft tissue/lymph node metastases, p < 0.001, Notch3-high in visceral, peritoneal/pleural and soft tissue/lymph node metastases, p < 0.001). Our study points to the MAPK and cMET axes as crucial in defining cancer progression and outcome in CUP patients and, if validated, could justify attempts at their therapeutic modulation.
机译:未知原发癌(CUP)是异质性实体,根据“一刀切”的治疗理念进行管理;迫切需要了解CUP的分子生物学。我们使用组织芯片回顾性研究了100例CUP肿瘤中Notch1、2、3,Jagged1,cMET和pMAPK生物分子的免疫组化(IHC)表达,旨在研究它们与临床病理特征和患者预后的相关性。 Notch3和pMAPK最常表达(分别为97%和91%)。发现Notch3与cMET表达呈线性相关性(p = 0.001),而pMAPK成为主要的不良预后因素(中位总生存OS 9 vs. 17个月,p = 0.016),也具有明显的阳性预测值(p = 0.02)。我们的研究表明,在单变量(中位OS 15 vs. 9个月,p = 0.05)和多变量分析(死亡的相对风险RR 0.48,p = 0.025)中,cMET表达在CUP中均具有良好的预后影响。在鳞癌中发现cMET和Notch3表达在统计学上更为频繁(阳性率为90%),并伴有独特的转移性IHC模式(软组织/淋巴结转移中cMET高,p <0.001,Notch3高。内脏,腹膜/胸膜和软组织/淋巴结转移,p <0.001)。我们的研究指出,MAPK和cMET轴对于定义CUP患者的癌症进展和预后至关重要,并且如果得到验证,可以证明其治疗调制的合理性。

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