肿瘤细胞中FSP-1的表达与非转移性结直肠癌的长期肿瘤预后有关。

Sun Bin Im, Jae Min Cho, Han Byul Kim, Dong-Hoon Shin, Myeong Sook Kwon, In Young Lee, Gyung Mo Son
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引用次数: 0

摘要

目的:最近的研究表明,癌症相关成纤维细胞(CAF)激活生物标志物在癌细胞中的表达与某些类型恶性肿瘤患者的临床预后相关。然而,CAF活化生物标志物的表达是否影响结直肠癌(CRC)的预后尚未完全阐明。本研究旨在评估伴有癌症侵袭的癌细胞中CAF活化生物标志物的表达与结直肠癌患者长期肿瘤预后之间的关系。方法:对135例I-III期结直肠癌患者的肿瘤标本进行免疫组化染色,检测成纤维细胞特异性蛋白-1 (FSP-1)、成纤维细胞活化蛋白α (FAPα)、α-平滑肌肌动蛋白(α- sma)和波形蛋白在癌细胞中的表达。结果:FSP-1在癌细胞中的表达与淋巴浸润、神经周围浸润、肿瘤(T)状态和淋巴结(N)状态显著相关。FAPα在癌细胞中的表达与淋巴浸润显著相关。在单因素和多因素分析中,FSP-1和α-SMA在癌细胞中的表达分别与较短的10年总生存期(OS)和较高的10年全身复发率(SR)相关。肿瘤出芽与较短的10年OS相关。然而,在本研究中,FAPα和vimentin对预后没有影响。结论:本研究发现FSP-1在肿瘤细胞中的表达与肿瘤侵袭有关。此外,FSP-1和α-SMA在癌细胞中的表达分别与10年OS和SR相关。因此,这些标志物可作为结直肠癌患者长期肿瘤预后的预测指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

FSP-1 expression in cancer cells is relevant to long-term oncological outcomes in nonmetastatic colorectal cancer.

FSP-1 expression in cancer cells is relevant to long-term oncological outcomes in nonmetastatic colorectal cancer.

FSP-1 expression in cancer cells is relevant to long-term oncological outcomes in nonmetastatic colorectal cancer.

FSP-1 expression in cancer cells is relevant to long-term oncological outcomes in nonmetastatic colorectal cancer.

Purpose: Recent studies have revealed that the expression of cancer-associated fibroblast (CAF) activation biomarkers in cancer cells is associated with clinical outcomes in patients with certain types of malignant tumors. However, whether the expression of CAF activation biomarkers affects the prognosis of colorectal cancer (CRC) has not been fully elucidated. This study aimed to evaluate the association between the expression of CAF activation biomarkers in cancer cells with cancer invasion and long-term oncological outcomes in patients with CRC.

Methods: Cancer specimens obtained from 135 patients with stage I-III CRC were examined using immunohistochemical staining to evaluate the expression of fibroblast specific protein-1 (FSP-1), fibroblast activation protein α (FAPα), α-smooth muscle actin (α-SMA), and vimentin in cancer cells.

Results: FSP-1 expression in cancer cells was significantly associated with lymphatic invasion, perineural invasion, tumor (T) status, and lymph node (N) status. FAPα expression in cancer cells was significantly associated with lymphatic invasion. On univariate and multivariate analyses, FSP-1 and α-SMA expression in cancer cells were associated with a short 10-year overall survival (OS) and high 10-year systemic recurrence (SR), respectively. Tumor budding was associated with a short 10-year OS. However, FAPα and vimentin did not contribute to the prognosis in this study.

Conclusion: In this study, we found that FSP-1 expression in cancer cells was related to cancer invasion. Additionally, FSP-1 and α-SMA expression in cancer cells was associated with 10-year OS and SR, respectively. Therefore, these markers may be used as predictors of long-term oncological outcomes in patients with CRC.

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