Yamamoto Shinji, Tomita Yasuhiko, Hoshida Yoshihiko, Takiguchi Shuji, Fujiwara Yoshiyuki, Yasuda Takushi, Yano Masahiko, Nakamori Shoji, Sakon Masato, Monden Morito, Aozasa Katsuyuki
Department of Pathology, Osaka University Graduate School of Medicine, Japan.
J Clin Oncol. 2003 Jul 1;21(13):2537-44. doi: 10.1200/JCO.2003.12.102.
Valosin-containing protein (VCP; also known as p97) was shown to be associated with antiapoptotic function and metastasis via activation of nuclear factor kappa-B signaling pathway. In this study, association of VCP expression with recurrence of gastric carcinoma (GC), in which lymphatic vessels are the main route of spread, was examined.
VCP expression in 330 patients with GC (242 males and 88 females) with ages ranging from 26 to 81 years (median, 60 years) was analyzed by immunohistochemistry, in which staining intensity in tumor cells was categorized as weaker (level 1) or equal to or stronger (level 2) than that in endothelial cells.
Ninety-four (28.7%) patient cases showed level 1 and 233 patient cases (71.3%) showed level 2 VCP expression. Patients with level 2 expression showed higher rates of large tumor size (P <.0001), undifferentiated histologic subtype (P <.05), presence of vascular and lymphatic invasion (P <.0001 for both), presence of lymph node metastasis (P <.0001), deep tumor invasion (P <.0001), and poorer disease-free and overall survivals (P <.0001 for both) compared with those with level 1 VCP expression. Multivariate analysis revealed VCP expression level as an independent prognosticator for disease-free and overall survival. VCP level was an indicator for disease-free and overall survival in the early (pT1; P <.01 and P <.05, respectively) and advanced (pT2-4; P <.05 for both) group of pathologic tumor-node-metastasis system classification.
The prognostic significance of VCP expression level in GC was demonstrated.
含缬酪肽蛋白(VCP;也称为p97)已被证明通过激活核因子κB信号通路与抗凋亡功能和转移相关。在本研究中,检测了VCP表达与胃癌(GC)复发的相关性,其中淋巴管是主要的扩散途径。
采用免疫组织化学方法分析了330例GC患者(242例男性和88例女性)的VCP表达,其中肿瘤细胞的染色强度分为比内皮细胞弱(1级)或等于或强于内皮细胞(2级)。
94例(28.7%)患者病例显示为1级,233例(71.3%)患者病例显示为2级VCP表达。与1级VCP表达的患者相比,2级表达的患者表现出更高的大肿瘤尺寸发生率(P<.0001)、未分化组织学亚型发生率(P<.05)、血管和淋巴管侵犯发生率(两者均P<.0001)、淋巴结转移发生率(P<.0001)、肿瘤深层侵犯发生率(P<.0001)以及无病生存期和总生存期较差(两者均P<.0001)。多变量分析显示VCP表达水平是无病生存期和总生存期的独立预后指标。在病理肿瘤-淋巴结-转移系统分类的早期(pT1;分别为P<.01和P<.05)和晚期(pT2-4;两者均为P<.05)组中,VCP水平是无病生存期和总生存期的指标。
证实了VCP表达水平在GC中的预后意义。