Hammoud Ghassan M, Ibdah Jamal A
Division of Gastroenterology and Hepatology, Department of Internal Medicine, School of Medicine, University of Missouri, One Hospital Drive, Columbia, MO 65212, USA.
Hepatobiliary Surg Nutr. 2016 Apr;5(2):188-90. doi: 10.3978/j.issn.2304-3881.2016.01.06.
Hepatocellular carcinoma (HCC) is a highly heterogenous disease and intratumor heterogeneity is a well-known fact within each individual tumor, and may involve morphological, immunohistochemical, and molecular heterogeneities. Understanding of intratumor heterogeneity of HCC should provide critical knowledge about prognosis of the disease and response to therapy. In a recent article by Friemel and colleagues, the investigators utilized a comprehensive approach in linking immunohistochemical markers and molecular changes to morphological intratumor heterogeneity in HCC. The study found that intratumor heterogeneity was detectable in 87% of HCC cases. Combined heterogeneities with respect to morphologic, immunohistochemical, and mutational status of the two most important driver mutations CTNNB1 and TP53 were seen in 22% of HCC cases. The study demonstrates the challenges facing therapeutic strategies targeting single molecules and may explain the limited success so far in developing molecular targeted therapy for HCC.
肝细胞癌(HCC)是一种高度异质性疾病,肿瘤内异质性在每个个体肿瘤中都是一个众所周知的事实,并且可能涉及形态学、免疫组织化学和分子异质性。了解HCC的肿瘤内异质性应能提供有关该疾病预后和治疗反应的关键知识。在Friemel及其同事最近发表的一篇文章中,研究人员采用了一种综合方法,将免疫组织化学标记物和分子变化与HCC的形态学肿瘤内异质性联系起来。该研究发现,87%的HCC病例中可检测到肿瘤内异质性。在22%的HCC病例中观察到了关于两种最重要的驱动突变CTNNB1和TP53的形态学、免疫组织化学和突变状态的联合异质性。该研究证明了针对单一分子的治疗策略所面临的挑战,并可能解释了迄今为止HCC分子靶向治疗取得有限成功的原因。