Im Sun Bin, Cho Jae Min, Kim Han Byul, Shin Dong-Hoon, Kwon Myeong Sook, Lee In Young, Son Gyung Mo
Department of Medicine, Pusan National University School of Medicine, Yangsan, Korea.
Department of Pathology, Pusan National University Yangsan Hospital, Yangsan, Korea.
Korean J Clin Oncol. 2022 Dec;18(2):66-77. doi: 10.14216/kjco.22009. Epub 2022 Dec 30.
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.
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.
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.
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.
近期研究表明,癌细胞中癌症相关成纤维细胞(CAF)激活生物标志物的表达与某些类型恶性肿瘤患者的临床结局相关。然而,CAF激活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。本研究旨在评估癌细胞中CAF激活生物标志物的表达与CRC患者癌症侵袭及长期肿瘤学结局之间的关联。
对135例I-III期CRC患者的癌组织标本进行免疫组织化学染色,以评估癌细胞中成纤维细胞特异性蛋白-1(FSP-1)、成纤维细胞激活蛋白α(FAPα)、α-平滑肌肌动蛋白(α-SMA)和波形蛋白的表达。
癌细胞中FSP-1的表达与淋巴侵犯、神经侵犯、肿瘤(T)分期和淋巴结(N)分期显著相关。癌细胞中FAPα的表达与淋巴侵犯显著相关。单因素和多因素分析显示,癌细胞中FSP-1和α-SMA的表达分别与10年总生存期(OS)缩短和10年全身复发(SR)率升高相关。肿瘤芽生与10年OS缩短相关。然而,在本研究中FAPα和波形蛋白对预后无影响。
在本研究中,我们发现癌细胞中FSP-1的表达与癌症侵袭相关。此外,癌细胞中FSP-1和α-SMA的表达分别与10年OS和SR相关。因此这些标志物可作为CRC患者长期肿瘤学结局的预测指标。