Girisa Sosmitha, Hegde Mangala, Harsha Choudhary, Manteghi Nafiseh, Longkumer Imliwati, Ahmed Gazi Naseem, Baruah Munindra Narayan, Kaul Sunil C, Wadhwa Renu, Kunnumakkara Ajaikumar B
Cancer Biology Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati (IITG), Guwahati 781039, Assam, India.
North-East Cancer Hospital and Research Institute, Guwahati 781023, Assam, India.
Cancers (Basel). 2025 Aug 30;17(17):2860. doi: 10.3390/cancers17172860.
Oral cancer remains a significant global health concern due to its high incidence and mortality, as highlighted by GLOBOCAN 2022, and is characterized by poor survival rates despite available therapies. Therefore, there is an imperative need for developing novel therapeutic targets for this disease.
This study investigates the oncogenic role of mortalin in oral cancer. We have used The Cancer Genome Atlas (TCGA) dataset, samples from North Eastern Region of India and tissue microarray to examine the expression of this gene/protein in patient samples. siRNA related knock down studies were carried out to determine the role of mortalin on oral cancer cell proliferation, survival, metastases, EMT, autophagy etc. Results: Analysis of TCGA dataset revealed increased mortalin expression in head and neck squamous cell carcinoma (HNSCC), which correlated with tumor grade and stage, and was associated with diminished overall survival. These findings were validated in oral cancer patient tissue samples obtained from the North East Region of India and oral cancer cell lines. Functional assays showed that mortalin knockdown via siRNA reduced cancer cell proliferation, migration, invasion, and angiogenesis while inducing apoptosis, disrupting mitochondrial membrane potential, and modulating autophagy. These effects were linked to altered expression of regulatory molecules, including p53, p21WAF1, cyclins, caspases, MMPs, Survivin, and components of the Akt/mTOR pathway, thereby alleviating key hallmarks of oral cancer.
Collectively, these data support mortalin as a potential therapeutic target for oral cancer and warrant further studies for the development of mortalin-targeting drugs in both laboratory and clinical settings.
正如《2022年全球癌症负担报告》所强调的,口腔癌因其高发病率和死亡率仍然是一个重大的全球健康问题,并且尽管有可用的治疗方法,其生存率仍很低。因此,迫切需要为这种疾病开发新的治疗靶点。
本研究调查了mortalin在口腔癌中的致癌作用。我们使用了癌症基因组图谱(TCGA)数据集、来自印度东北地区的样本和组织芯片来检测该基因/蛋白在患者样本中的表达。进行了与小干扰RNA(siRNA)相关的敲低研究,以确定mortalin对口腔癌细胞增殖、存活、转移、上皮-间质转化(EMT)、自噬等的作用。结果:对TCGA数据集的分析显示,mortalin在头颈部鳞状细胞癌(HNSCC)中的表达增加,这与肿瘤分级和分期相关,并且与总生存期缩短有关。这些发现在从印度东北地区获得的口腔癌患者组织样本和口腔癌细胞系中得到了验证。功能分析表明,通过siRNA敲低mortalin可降低癌细胞的增殖、迁移、侵袭和血管生成,同时诱导细胞凋亡、破坏线粒体膜电位并调节自噬。这些作用与包括p53、p21WAF1、细胞周期蛋白、半胱天冬酶、基质金属蛋白酶、生存素以及Akt/mTOR通路成分在内的调节分子的表达改变有关,从而减轻了口腔癌的关键特征。
总体而言,这些数据支持mortalin作为口腔癌的潜在治疗靶点,并值得在实验室和临床环境中进一步开展研究以开发针对mortalin的药物。