Integrating Clinical and Molecular Insights: CTPS1 as a Key Biomarker of Tumor Progression and Prognosis in Colorectal Adenocarcinoma.

IF 1.2
Dina Moustafa Thabit, Rofida Khalifa, Dalia M Thabet
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Abstract

Colorectal cancer (CRC) remains a leading cause of global cancer-related mortality. Cytidine triphosphate synthase 1 (CTPS1) is an essential enzyme for DNA synthesis and cell cycle progression. While CTPS1 has been implicated in the pathogenesis of various malignancies, its clinical significance in colorectal adenocarcinoma remains poorly defined. This study aimed to investigate the immunohistochemical (IHC) expression of CTPS1 in colorectal adenocarcinoma and evaluate its association with clinicopathological features and survival outcomes. CTPS1 expression was assessed via IHC in 168 colorectal adenocarcinoma specimens and 142 matched adjacent non-neoplastic tissues. Statistical associations with clinicopathological parameters were analyzed using χ2 or Fisher exact tests. Progression-free survival (PFS) and disease-free survival (DFS) were estimated using the Kaplan-Meier method and compared via the log-rank test. Multivariate Cox proportional hazards regression was employed to identify independent prognostic factors. CTPS1 expression was significantly upregulated in tumour tissues compared with adjacent normal mucosa (P<0.001). High CTPS1 expression was observed in 55.4% of tumor samples and significantly correlated with advanced T stage, TNM stage, and modified Dukes staging, as well as nodal involvement, distant metastasis, tumor recurrence, and elevated serum CEA levels. Furthermore, elevated CTPS1 was associated with aggressive histologic features, including higher grade, tumor budding, poorly differentiated clusters (PDCs), and tumor deposits. Both PFS and DFS were significantly shorter in patients with high CTPS1 expression (P<0.001). Multivariate analysis confirmed that high CTPS1 expression, along with nodal status and tumor recurrence, was an independent prognostic factor for both PFS and DFS. Therefore, CTPS1 is a robust independent prognostic indicator and a marker of aggressive progression in colorectal adenocarcinoma. These findings suggest that CTPS1 is a promising biomarker for risk stratification and may guide clinical decision-making in the management of CRC.

整合临床和分子洞察:CTPS1作为结直肠癌肿瘤进展和预后的关键生物标志物。
结直肠癌(CRC)仍然是全球癌症相关死亡的主要原因。胞苷三磷酸合成酶1 (Cytidine triphosphate synthase 1, CTPS1)是DNA合成和细胞周期进程的重要酶。虽然CTPS1与多种恶性肿瘤的发病机制有关,但其在结直肠癌中的临床意义仍不明确。本研究旨在探讨CTPS1在结直肠癌中的免疫组化表达,并评估其与临床病理特征和生存结局的关系。通过免疫组化检测168例结直肠癌标本和142例匹配的邻近非肿瘤组织中CTPS1的表达。采用χ2或Fisher精确检验分析与临床病理参数的统计学相关性。使用Kaplan-Meier法估计无进展生存期(PFS)和无病生存期(DFS),并通过log-rank检验进行比较。采用多因素Cox比例风险回归确定独立预后因素。CTPS1在肿瘤组织中的表达与邻近正常粘膜相比显著上调(P
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