Abdel-Maksoud Mostafa A, Ullah Sajid, Nadeem Amun, Shaikh Aisha, Zia Muhammad Khurram, Zakri Adel M, Almanaa Taghreed N, Alfuraydi Akram A, Mubarak Ayman, Hameed Yasir
Department of Botany and Microbiology, College of Science, King Saud University P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Badr Al Samma Hospital Barka 320, Oman.
Am J Transl Res. 2024 Jan 15;16(1):63-74. doi: 10.62347/TWOY1681. eCollection 2024.
Cancer, a formidable disease, continues to challenge our understanding and therapeutic approaches. This study delves into the pan-cancer analysis of BCL2 Associated X (BAX) gene expression, seeking to unravel its significance in cancer development, prognosis, and potential therapeutic strategies.
A combination of bioinformatics and molecular experiments.
Our pan-cancer investigation into BAX expression encompassed 33 distinct cancer types, revealing a remarkable and uniform increase in BAX expression. This groundbreaking finding emphasizes the potential universality of BAX's role in cancer development and progression. Further, our study explored the prognostic implications of BAX expression, highlighting a consistent association between up-regulated BAX and poor overall survival (OS) in Liver Hepatocellular Carcinoma (LIHC) and Skin Cutaneous Melanoma (SKCM). These results suggest that BAX may serve as an adverse prognostic indicator in these malignancies, emphasizing the importance of personalized treatment strategies. Epigenetic and genetic analyses of BAX provided valuable insights. Hypomethylation of the BAX promoter region was evident in LIHC and SKCM, which likely contributes to the up-regulation of BAX, while genetic mutations in the BAX gene itself were infrequent in these cancers. Our exploration of BAX-associated signaling pathways and the correlation between BAX expression and CD8+ T cell infiltration shed light on the intricate molecular landscape of cancer. BAX's interaction with key apoptotic and immune-related pathways reinforces its role as a central player in tumor development and the immune microenvironment. Moreover, our drug prediction analysis identified potential therapeutic agents for modulating BAX expression in the context of LIHC and SKCM, bridging the gap between research and clinical application.
In sum, our comprehensive BAX study not only enhances our understanding of its significance as a biomarker gene but also offers novel avenues for therapeutic interventions, contributing to the ongoing quest for more effective cancer treatments and improved patient care.
癌症是一种可怕的疾病,持续挑战着我们的理解和治疗方法。本研究深入探讨BCL2相关X(BAX)基因表达的泛癌分析,旨在揭示其在癌症发生、预后及潜在治疗策略中的意义。
生物信息学与分子实验相结合。
我们对BAX表达的泛癌研究涵盖33种不同癌症类型,发现BAX表达显著且一致地增加。这一开创性发现强调了BAX在癌症发生和进展中作用的潜在普遍性。此外,我们的研究探讨了BAX表达的预后意义,突出了BAX上调与肝细胞肝癌(LIHC)和皮肤黑色素瘤(SKCM)中较差的总生存期(OS)之间的一致关联。这些结果表明,BAX可能是这些恶性肿瘤中的不良预后指标,强调了个性化治疗策略的重要性。对BAX的表观遗传和基因分析提供了有价值的见解。BAX启动子区域的低甲基化在LIHC和SKCM中明显,这可能导致BAX上调,而BAX基因本身的基因突变在这些癌症中并不常见。我们对与BAX相关的信号通路以及BAX表达与CD8 + T细胞浸润之间相关性的探索,揭示了癌症复杂的分子格局。BAX与关键凋亡和免疫相关通路的相互作用强化了其作为肿瘤发生和免疫微环境核心参与者的作用。此外,我们的药物预测分析确定了在LIHC和SKCM背景下调节BAX表达的潜在治疗药物,弥合了研究与临床应用之间的差距。
总之,我们对BAX的全面研究不仅加深了我们对其作为生物标志物基因重要性的理解,还为治疗干预提供了新途径,有助于不断寻求更有效的癌症治疗方法并改善患者护理。