Park Min Jee, Baek Hae Woon, Rhee Ye-Young, Lee Cheol, Park Jeong Whan, Kim Hwal Woong, Moon Kyung Chul
Department of Pathology, Seoul National University College of Medicine, Seoul, Korea.
Department of Pathology, Good Moonhwa Hospital, Busan, Korea.
J Pathol Transl Med. 2015 Jan;49(1):37-43. doi: 10.4132/jptm.2014.10.25. Epub 2015 Jan 15.
A few recent studies have demonstrated a possible role of transglutaminase 2 (TG2) in tumorigenesis or progression of renal cell carcinoma (RCC). The aim of this study was to examine TG2 expression and its clinicopathologic significance in a large number of human clear cell RCCs (CCRCCs).
We analyzed 638 CCRCC patients who underwent partial or radical nephrectomy between 1995 and 2005. The expression of TG2 was determined by immunohistochemistry and categorized into four groups, according to staining intensity: negative (0), mild (1+), moderate (2+), and strong (3+).
TG2 staining intensity was negative in 8.5% of CCRCC (n=54), 1+ in 32.6% (n=208), 2+ in 50.5% (n=322), and 3+ in 8.5% (n=54). Strong TG2 expression was correlated with high Fuhrman nuclear grade (p=.011), high T category (p=.049), metastasis (p=.043) and male sex (p<.001) but not with N category.The survival analysis showed a significant association between strong TG2 expression and worse overall and cancer-specific survival (p=.027 and p=.010, respectively). On multivariate analysis, strong TG2 expression was a marginally significant prognostic indicator for Fuhrman nuclear grade and TNM staging (p=.054).
Our study is the first to demonstrate the clinicopathologic significance of TG2 expression in a large number of human CCRCC samples. Strong TG2 expression was associated with high nuclear grade and poor prognosis.
最近的一些研究表明,转谷氨酰胺酶2(TG2)在肾细胞癌(RCC)的肿瘤发生或进展中可能发挥作用。本研究的目的是检测大量人类透明细胞肾细胞癌(CCRCC)中TG2的表达及其临床病理意义。
我们分析了1995年至2005年间接受部分或根治性肾切除术的638例CCRCC患者。通过免疫组织化学测定TG2的表达,并根据染色强度分为四组:阴性(0)、轻度(1+)、中度(2+)和强阳性(3+)。
CCRCC中TG2染色强度为阴性的占8.5%(n = 54),1+的占32.6%(n = 208),2+的占50.5%(n = 322),3+的占8.5%(n = 54)。TG2强表达与高Fuhrman核分级(p = 0.011)、高T分期(p = 0.049)、转移(p = 0.043)和男性性别(p < 0.001)相关,但与N分期无关。生存分析显示,TG2强表达与总体生存率和癌症特异性生存率较差显著相关(分别为p = 0.027和p = 0.010)。多因素分析显示,TG2强表达是Fuhrman核分级和TNM分期的边缘显著预后指标(p = 0.054)。
我们的研究首次证明了TG2表达在大量人类CCRCC样本中的临床病理意义。TG2强表达与高核分级和不良预后相关。