Yamaguchi Arisa, Yokobori Takehiko, Sohda Makoto, Watanabe Takayoshi, Nakazawa Nobuhiro, Sano Akihiko, Sakai Makoto, Shiraishi Takuya, Motegi Sei-Ichiro, Shirabe Ken, Saeki Hiroshi
Department of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Division of Gene Therapy Science, Initiative for Advanced Research (GIAR), Gunma University, Maebashi, Gunma, Japan.
Ann Surg Oncol. 2025 Apr 10. doi: 10.1245/s10434-025-17238-4.
Esophageal squamous cell carcinoma (ESCC) is a significant cause of cancer-related death despite advances in multidisciplinary treatment. Transcriptional intermediary factor 1 γ (TIF1γ) has been known to be involved in tumorigenesis and epithelial-mesenchymal transition (EMT), which are linked to cancer aggressiveness and therapeutic resistance. However, its role in ESCC remains unclear. Therefore, we investigated the expression significance and function of TIF1γ in ESCC.
We used immunohistochemical analysis to investigate the clinical significance of tumoral TIF1γ expression in 131 patients with ESCC. We also performed in vitro analysis using ESCC cell lines to evaluate the effects of TIF1γ suppression on EMT marker expression, migration ability, and 5-fluorouracil (5-FU) sensitivity.
The TIF1γ protein was mainly expressed in the nuclear ESCC cells. Low nuclear TIF1γ expression was associated with the progression of tumor depth and frequent recurrence. Low TIF1γ expression was an independent predictor of recurrence in ESCC. Moreover, suppression of TIF1γ facilitated EMT-like changes, such as high migration ability, E-cadherin suppression, vimentin induction, and 5-FU resistance of ESCC cells.
TIF1γ may be a promising biomarker for predicting patients with ESCC at high risk of recurrence. Therapeutic strategies that induce TIF1γ expression are expected to improve the chemosensitivity and prognosis of high-risk patients with ESCC who have low TIF1γ.
尽管多学科治疗取得了进展,但食管鳞状细胞癌(ESCC)仍是癌症相关死亡的重要原因。已知转录中介因子1γ(TIF1γ)参与肿瘤发生和上皮-间质转化(EMT),这与癌症侵袭性和治疗耐药性有关。然而,其在ESCC中的作用仍不清楚。因此,我们研究了TIF1γ在ESCC中的表达意义和功能。
我们采用免疫组化分析方法,研究131例ESCC患者肿瘤组织中TIF1γ表达的临床意义。我们还使用ESCC细胞系进行体外分析,以评估TIF1γ抑制对EMT标志物表达、迁移能力和5-氟尿嘧啶(5-FU)敏感性的影响。
TIF1γ蛋白主要表达于ESCC细胞核中。细胞核TIF1γ低表达与肿瘤深度进展和频繁复发相关。TIF1γ低表达是ESCC复发的独立预测因素。此外,抑制TIF1γ可促进EMT样变化,如ESCC细胞的高迁移能力、E-钙黏蛋白抑制、波形蛋白诱导和5-FU耐药。
TIF1γ可能是预测ESCC复发高危患者的一个有前景的生物标志物。诱导TIF1γ表达的治疗策略有望改善TIF1γ低表达的ESCC高危患者的化疗敏感性和预后。