Department of Comparative Medicine, Laboratory Animal Center, Dalian Medical University, Dalian, 116044, Liaoning, China.
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Biochemistry and Molecular Biology, Peking University Cancer Hospital & Institute, No. 52 Fucheng Road, Beijing, 100142, China.
Biol Sex Differ. 2020 Aug 13;11(1):46. doi: 10.1186/s13293-020-00316-5.
Hepatocellular carcinoma (HCC) is the most common liver cancer and is highly malignant. Male prevalence and frequent activation of the Ras signaling pathway are distinct characteristics of HCC. However, the underlying mechanisms remain to be elucidated. By exploring Hras12V transgenic mice showing male-biased hepatocarcinogenesis, we performed a high-throughput comparative proteomic analysis based on tandem-mass-tag (TMT) labeling combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS) on the tissue samples obtained from HCC (T) and their paired adjacent precancerous (P) of Hras12V transgenic male and female mice (Ras-Tg) and normal liver (W) of wild-type male and female mice (Non-Tg). The further validation and investigation were performed using quantitative real-time PCR and western blot. Totally, 5193 proteins were quantified, originating from 5733 identified proteins. Finally, 1344 differentially expressed proteins (DEPs) (quantified in all examined samples; |ratios| ≥ 1.5, p < 0.05) were selected for further analysis. Comparison within W, P, and T of males and females indicated that the number of DEPs in males was much higher than that in females. Bioinformatics analyses showed the common and unique cluster-enriched items between sexes, indicating the common and gender-disparate pathways towards HCC. Expression change pattern analysis revealed HCC positive/negative-correlated and ras oncogene positive/negative-correlated DEPs and pathways. In addition, it showed that the ras oncogene gradually and significantly reduced the responses to sex hormones from hepatocytes to hepatoma cells and therefore shrunk the gender disparity between males and females, which may contribute to the cause of the loss of HCC clinical responses to the therapeutic approaches targeting sex hormone pathways. Additionally, gender disparity in the expression levels of key enzymes involved in retinol metabolism and terpenoid backbone/steroid biosynthesis pathways may contribute to male prevalence in hepatocarcinogenesis. Further, the biomarkers, SAA2, Orm2, and Serpina1e, may be sex differences. In conclusion, common and unique DEPs and pathways toward HCC initiated by ras oncogene from sexually dimorphic hepatocytes provide valuable and novel insights into clinical investigation and practice.
肝细胞癌 (HCC) 是最常见的肝癌,恶性程度很高。男性患病率和 Ras 信号通路的频繁激活是 HCC 的显著特征。然而,其潜在机制仍有待阐明。通过探索雄性偏倚性肝癌发生的 Hras12V 转基因小鼠,我们对 Hras12V 转基因雄性和雌性小鼠 (Ras-Tg) 的 HCC (T) 及其配对的癌前组织 (P) 与野生型雄性和雌性小鼠 (Non-Tg) 的正常肝组织 (W) 进行了基于串联质量标签 (TMT) 标记与液相色谱-串联质谱联用 (LC-MS/MS) 的高通量比较蛋白质组学分析。进一步采用定量实时 PCR 和 Western blot 进行验证和研究。共定量了 5193 种蛋白质,源自 5733 种鉴定的蛋白质。最后,选择了 1344 个差异表达蛋白 (DEPs)(在所有检测样本中定量;|比值|≥1.5,p<0.05) 进行进一步分析。雄性和雌性的 W、P 和 T 之间的比较表明,雄性中的 DEP 数量远高于雌性。生物信息学分析显示了性别间常见和独特的聚类富集项目,表明了 HCC 发生的共同和性别差异途径。表达变化模式分析揭示了 HCC 阳性/阴性相关和 ras 癌基因阳性/阴性相关的 DEPs 和途径。此外,它表明 ras 癌基因逐渐且显著地降低了雄性向肝癌细胞的肝细胞对性激素的反应,从而缩小了雄性和雌性之间的性别差异,这可能有助于解释 HCC 对靶向性激素途径的治疗方法的临床反应丧失的原因。此外,视黄醇代谢和萜烯骨架/类固醇生物合成途径中关键酶的表达水平的性别差异可能导致肝癌发生中的男性患病率。此外,SAA2、Orm2 和 Serpina1e 等生物标志物可能存在性别差异。总之,ras 癌基因从性别二态性肝细胞引发的 HCC 的常见和独特的 DEPs 和途径为临床研究和实践提供了有价值的新见解。