Ranjpour Maryam, Wajid Saima, Jain Swatantra Kumar
Departmentof Biotechnology, School of Chemical and Life Sciences, Jamia Hamdard, New Delhi, 110062, India.
Department of Medical Biochemistry, HIMSR, Jamia Hamdard, New Delhi, 110062, India.
Protoplasma. 2021 Sep;258(5):1133-1143. doi: 10.1007/s00709-021-01632-2. Epub 2021 Mar 8.
Hepatocellular carcinoma (HCC) is one of the most common cancers associated with high mortality rate. Understanding of events leading to HCC pathophysiology is essential for its better management. We earlier reported development of a novel rodent model by administrating chemical carcinogens, DEN, and 2-AAF for study of HCC at very early stage. 2D-Electrophoresis analysis of total serum proteins identified several differentially expressed proteins in animals undergoing tumorigenesis. MALDI-TOF-MS/MS analyses were performed to characterize the differentially expressed proteins. Further real-time PCR analyses were taken place to quantify the transcript expression for the identified proteins at HCC initiation and tumor stages. Considering protein-protein interactions among the experimentally identified proteins and their interacting neighbors, a protein network has been analyzed that provided further insight into molecular events taking place during HCC development. Histological changes confirmed HCC initiation and hepatotumorigenesis at 1 and 4 months post carcinogen treatment, respectively. Four differentially expressed proteins were identified which were further characterized as regulator of G protein signaling 1 (RGS1), sepiapterin reductase (SPR), similar to zinc finger and BTB domain-containing protein 21 isoform X2 (ZNF295), and a hypothetical protein CXorf58 homolog. Quantification of transcripts for these proteins revealed elevation in their expression both at initiation and tumorigenesis stages. The study deciphers the regulatory role of these proteins during HCC progression.
肝细胞癌(HCC)是最常见的癌症之一,死亡率很高。了解导致HCC病理生理学的事件对于更好地管理该病至关重要。我们之前报道了通过给予化学致癌物二乙基亚硝胺(DEN)和2-乙酰氨基芴(2-AAF)建立一种新型啮齿动物模型,用于研究HCC的极早期阶段。对全血清蛋白进行二维电泳分析,确定了在发生肿瘤的动物中有几种差异表达的蛋白。进行基质辅助激光解吸电离飞行时间串联质谱(MALDI-TOF-MS/MS)分析以表征差异表达的蛋白。进一步进行实时聚合酶链反应(PCR)分析,以量化在HCC起始和肿瘤阶段所鉴定蛋白的转录本表达。考虑到实验鉴定的蛋白与其相互作用的邻近蛋白之间的蛋白质-蛋白质相互作用,分析了一个蛋白质网络,该网络为HCC发展过程中发生的分子事件提供了进一步的见解。组织学变化分别在致癌物处理后1个月和4个月证实了HCC的起始和肝肿瘤发生。鉴定出四种差异表达的蛋白,它们进一步被表征为G蛋白信号调节因子1(RGS1)、蝶啶还原酶(SPR)、类似于含锌指和BTB结构域蛋白21异构体X2(ZNF295)以及一种假定蛋白CXorf58同源物。对这些蛋白转录本的定量显示,它们在起始和肿瘤发生阶段的表达均升高。该研究揭示了这些蛋白在HCC进展过程中的调节作用。