Gupta Sameer, Garg Sudeep, Kumar Vijay, Chaturvedi Arun, Misra Sanjeev, Akhtar Naseem, Rajan Shiv, Kaur Jatinder, Lakshmanan Manikandan, Jain Kavitha
Department of Surgical Oncology, King George's Medical University, Lucknow, India.
AIIMS, Jodhpur, Rajasthan, India.
Ann Hepatobiliary Pancreat Surg. 2020 Nov 30;24(4):460-468. doi: 10.14701/ahbps.2020.24.4.460.
BACKGROUNDS/AIMS: Transglutaminase 2 (TG2) is known to be an important mediator of inflammation induced carcinogenesis pathway. Chronic inflammation is the most important causative factor in Gallbladder cancer (GBC) carcinogenesis. We analyzed the expression of TG2 in GBC and its role as potential prognostic marker, first of its kind study.
We analyzed TG2 expression in 100 cases of GBC and 28 cases of non-cancer gallbladder specimen (calculus cholecystitis). We studied TG2 expression in GBC in comparison to control group and evaluated its role as a potential prognostic marker.
TG2 score (1-9) was calculated by multiplying percentage cytoplasmic expression (P) with intensity of expression (I) in tumor cells. Positive TG-2 expression was observed in 62% of GBC patients compared to only 21% (n=6) in control group (=0.001). In curative resection subgroup (n=54), TG2 positive patients showed shorter disease free survival rate (=0.04) and higher rate of recurrence (=0.03) compared to TG2 negative patients. TG2 positive expression was observed in 15/16 of patients with recurrent disease. In palliative treatment subgroup, patients with strong TG2 positive expression had poorer disease specific survival (=0.01) as compared to weakly positive group. On multivariate analysis, lymph node status (=0.03) and TG2 expression (=0.037), were found to be significant predictor of recurrence and eventual survival.
Positive TG2 expression was related to higher recurrence rates post curative surgery, shorter disease free and overall survival and ultimately portended poor prognosis. It may be helpful in better prognostication and tailoring therapeutic approach for better management of GBC.
背景/目的:已知转谷氨酰胺酶2(TG2)是炎症诱导致癌途径的重要介质。慢性炎症是胆囊癌(GBC)致癌过程中最重要的致病因素。我们分析了TG2在GBC中的表达及其作为潜在预后标志物的作用,这是同类研究中的首例。
我们分析了100例GBC病例和28例非癌胆囊标本(结石性胆囊炎)中TG2的表达。我们研究了GBC中TG2的表达与对照组相比,并评估了其作为潜在预后标志物的作用。
TG2评分(1-9)通过将肿瘤细胞中细胞质表达百分比(P)与表达强度(I)相乘来计算。62%的GBC患者观察到TG-2阳性表达,而对照组仅为21%(n=6)(P=0.001)。在根治性切除亚组(n=54)中,与TG2阴性患者相比,TG2阳性患者的无病生存率较短(P=0.04),复发率较高(P=0.03)。15/16例复发病例中观察到TG2阳性表达。在姑息治疗亚组中,与弱阳性组相比,TG2强阳性表达的患者疾病特异性生存率较差(P=0.01)。多因素分析发现,淋巴结状态(P=0.03)和TG2表达(P=0.037)是复发和最终生存的重要预测因素。
TG2阳性表达与根治性手术后较高的复发率、较短的无病生存期和总生存期相关,最终预示预后不良。它可能有助于更好地进行预后评估和制定治疗方案,以更好地管理GBC。