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Clinicopathological and prognostic implications of endoglin (CD105) expression in hepatocellular carcinoma and its adjacent non-tumorous liver

机译:内皮糖蛋白(CD105)在肝细胞癌及其邻近非肿瘤肝脏中表达的临床病理和预后意义

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摘要

Aim: The expression pattern of endoglin (CD105) in hepatocellular carcinoma (HCC) has not been reported so far. We hypothesized that CD105 could differentially highlight a subset of microvessels in HCC, and intratumoral microvessel density (IMVD) by CD105 immunostaining (IMVD-CD105) could provide better prognostic information than IMVD by CD34 immunostaining (IMVD-CD34). Methods: Paraffin blocks of tumor and adjacent non-tumorous liver tissues from 86 patients who underwent curative resection of HCC were used for this study. Serial sections were stained for CD105 and CD34, respectively, to highlight the microvessels. IMVD was counted according to a standard protocol. Results: In the HCC tissues, CD105 was either negatively or positively stained only in a subset of microvessels. In contrast, CD34 showed positive and more extensive microvessel staining in all cases examined. However, in the adjacent non-tumorous liver sections, CD105 showed a diffuse pattern of microvessel staining in 20 of 86 cases, while CD34 showed negative or only focal staining of the sinusoids around portal area. Correlation with clinicopathological data demonstrated that lower scores of IMVD-CD105 were found in larger sized tumors [mean 41.4/0.74 mm 2 (>5 cm tumor) vs 65.9/0.74 mm 2 (≤5 cm tumor), P = 0.043] and more aggressive tumors, as indicated by venous infiltration [36.8/0.74 mm 2 (present) vs 64.2/0.74 mm 2 (absent), P = 0.020], microsatellite nodules [35.1/0.74 mm 2 (present) vs 65.9/0.74 mm 2 (absent), P = 0.012], and advanced TNM tumor stage [38.8/0.74 mm 2 (stage 3 or 4) vs 68.3/0.74 mm 2 (stage 1 or 2), P = 0.014]. No prognostic significance was observed when median values were used as cut-off points using either IMVD-CD105 or IMVD-CD34. However, the presence of the diffuse pattern of CD105 expression in the adjacent non-tumorous liver tissues predicted a poorer disease-free survival (median 8.6 vs 21.5 mo, P = 0.026). Conclusion: Our data demonstrate that a lower IMVD-CD105 is associated with larger and more aggressive tumors. In this study, IMVD-CD105 did not provide significant prognostic information. However, active angiogenesis as highlighted by diffuse CD105 staining of the microvessels in the adjacent non-tumorous liver tissues is predictive of early recurrence. © 2005 The WJG Press and Elsevier Inc. All rights reserved.
机译:目的:迄今为止尚未报道内皮糖蛋白(CD105)在肝细胞癌(HCC)中的表达模式。我们假设CD105可以差异显示肝癌中的微血管子集,而CD105免疫染色(IMVD-CD105)的肿瘤内微血管密度(IMVD)可以比CD34免疫染色(IMVD-CD34)的IMVD提供更好的预后信息。方法:本研究采用86例肝癌根治性切除术患者的肿瘤及邻近非肿瘤肝组织的石蜡块。连续切片分别对CD105和CD34染色,以突出微血管。根据标准协议对IMVD进行计数。结果:在肝癌组织中,CD105仅在部分微血管中被阴性或阳性染色。相反,在所有检查的病例中,CD34均显示阳性和更广泛的微血管染色。然而,在相邻的非肿瘤肝切片中,CD105在86例病例中有20例显示了微血管染色的弥散型,而CD34则在门脉区域周围显示了正弦波阴性或仅局灶性染色。与临床病理数据的相关性表明,在较大尺寸的肿瘤中发现较低的IMVD-CD105评分[平均41.4 / 0.74 mm 2(> 5 cm肿瘤)与65.9 / 0.74 mm 2(≤5cm肿瘤),P = 0.043]和更多侵袭性肿瘤,如静脉浸润[36.8 / 0.74 mm 2(存在)与64.2 / 0.74 mm 2(不存在),P = 0.020],微卫星结节[35.1 / 0.74 mm 2(存在)与65.9 / 0.74 mm 2( P = 0.012]和晚期TNM肿瘤分期[38.8 / 0.74 mm 2(3或4期)与68.3 / 0.74 mm 2(1或2期),P = 0.014]。当使用IMVD-CD105或IMVD-CD34将中值用作临界点时,未观察到预后意义。然而,在相邻的非肿瘤肝组织中CD105表达的弥散模式的存在预示着较差的无病生存期(中位数8.6对21.5 mo,P = 0.026)。结论:我们的数据表明,较低的IMVD-CD105与更大,更具侵袭性的肿瘤有关。在这项研究中,IMVD-CD105没有提供重要的预后信息。然而,如邻近非肿瘤肝组织中微血管的弥漫性CD105染色所强调的,主动血管生成可预示早期复发。 ©2005 WJG Press and Elsevier Inc.保留所有权利。

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