Hashemi Farideh, Tajik Fatemeh, Saeednejad Zanjani Leili, Dehghan Manshadi Masoumeh, Safaei Sadegh, Babaheidarian Pegah, Fattahi Fahimeh, Ghods Roya, Madjd Zahra
Oncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Department of Molecular Medicine, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran Iran.
Biomarkers. 2024 Dec;29(8):539-556. doi: 10.1080/1354750X.2024.2423270. Epub 2024 Nov 11.
Talin-1 (TLN1) is crucial in cell migration, metastasis, and cancer development. This study evaluated Talin-1 expression and its clinical significance in gastric cancer (GC), along with human epidermal growth factor receptor-2 (HER-2) expression and its correlation with Talin-1.
Bioinformatics analysis assessed the potential prognostic value of Talin-1 and HER-2 in GC patients. The study included 223 GC patients (Signet Ring Cells and Intestinal subtypes) and 29 non-malignant tissue samples. Immunohistochemistry (IHC) on tissue microarray slides evaluated Talin-1 and HER-2 expression and clinical significance. Receiver operating characteristic (ROC) curves assessed their diagnostic value.
Bioinformatics identified Talin-1 as a potential prognostic factor and HER-2 as an oncogene in GC. Talin-1 and HER-2 expression increased in SRC-type GC samples compared to non-malignant tissues. High cytoplasmic Talin-1 expression inversely correlated with tumor expansion and invasion in SRC-type GC. Increased HER-2 expression positively correlated with metastasis. ROC curves showed significant diagnostic values for both proteins.
Higher cytoplasmic Talin-1 expression is associated with less invasive tumor behavior, while increased membranous HER-2 expression is associated with metastasis in SRC-type GC. These findings suggest potential use in assessing diagnosis and screening high-risk cancer patients, particularly those with SRC-type GC.
踝蛋白-1(TLN1)在细胞迁移、转移及癌症发展过程中起关键作用。本研究评估了踝蛋白-1在胃癌(GC)中的表达及其临床意义,同时研究了人表皮生长因子受体-2(HER-2)的表达及其与踝蛋白-1的相关性。
生物信息学分析评估了踝蛋白-1和HER-2在GC患者中的潜在预后价值。该研究纳入了223例GC患者(印戒细胞型和肠型)及29例非恶性组织样本。通过组织微阵列玻片上的免疫组织化学(IHC)评估踝蛋白-1和HER-2的表达及其临床意义。采用受试者工作特征(ROC)曲线评估它们的诊断价值。
生物信息学分析确定踝蛋白-1为GC的潜在预后因子,HER-2为GC中的致癌基因。与非恶性组织相比,印戒细胞型GC样本中踝蛋白-1和HER-2的表达增加。在印戒细胞型GC中,高细胞质踝蛋白-1表达与肿瘤扩展和侵袭呈负相关。HER-2表达增加与转移呈正相关。ROC曲线显示这两种蛋白均具有显著的诊断价值。
在印戒细胞型GC中,较高的细胞质踝蛋白-1表达与肿瘤侵袭性较低相关,而膜性HER-2表达增加与转移相关。这些发现提示其在评估诊断及筛查高危癌症患者,尤其是印戒细胞型GC患者方面具有潜在应用价值。