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释放BCL-2相关蛋白家族的治疗潜力:探索BCL-2抑制剂在癌症治疗中的应用。

Unlocking the Therapeutic Potential of BCL-2 Associated Protein Family: Exploring BCL-2 Inhibitors in Cancer Therapy.

作者信息

Dakkak Bisan El, Taneera Jalal, El-Huneidi Waseem, Abu-Gharbieh Eman, Hamoudi Rifat, Semreen Mohammad H, Soares Nelson C, Abu-Rish Eman Y, Alkawareek Mahmoud Y, Alkilany Alaaldin M, Bustanji Yasser

机构信息

Research Institute of Medical and Health Sciences, University of Sharjah, Sharjah 27272, United Arab Emirates.

College of Medicine, University of Sharjah, Sharjah 27272, United Arab Emirates.

出版信息

Biomol Ther (Seoul). 2024 May 1;32(3):267-280. doi: 10.4062/biomolther.2023.149. Epub 2024 Apr 9.

Abstract

Apoptosis, programmed cell death pathway, is a vital physiological mechanism that ensures cellular homeostasis and overall cellular well-being. In the context of cancer, where evasion of apoptosis is a hallmark, the overexpression of anti-apoptotic proteins like Bcl2, Bcl-xL and Mcl-1 has been documented. Consequently, these proteins have emerged as promising targets for therapeutic interventions. The BCL-2 protein family is central to apoptosis and plays a significant importance in determining cellular fate serving as a critical determinant in this biological process. This review offers a comprehensive exploration of the BCL-2 protein family, emphasizing its dual nature. Specifically, certain members of this family promote cell survival (known as anti-apoptotic proteins), while others are involved in facilitating cell death (referred to as pro-apoptotic and BH3-only proteins). The potential of directly targeting these proteins is examined, particularly due to their involvement in conferring resistance to traditional cancer therapies. The effectiveness of such targeting strategies is also discussed, considering the tumor's propensity for anti-apoptotic pathways. Furthermore, the review highlights emerging research on combination therapies, where BCL-2 inhibitors are used synergistically with other treatments to enhance therapeutic outcomes. By understanding and manipulating the BCL-2 family and its associated pathways, we open doors to innovative and more effective cancer treatments, offering hope for resistant and aggressive cases.

摘要

细胞凋亡,即程序性细胞死亡途径,是一种重要的生理机制,可确保细胞内环境稳定和细胞整体健康。在癌症背景下,逃避细胞凋亡是一个标志,已有文献记载抗凋亡蛋白如Bcl2、Bcl-xL和Mcl-1的过度表达。因此,这些蛋白已成为有前景的治疗干预靶点。BCL-2蛋白家族在细胞凋亡中起核心作用,在决定细胞命运方面具有重要意义,是这一生物学过程的关键决定因素。本综述全面探讨了BCL-2蛋白家族,强调了其双重性质。具体而言,该家族的某些成员促进细胞存活(称为抗凋亡蛋白),而其他成员则参与促进细胞死亡(称为促凋亡蛋白和仅含BH3结构域的蛋白)。研究了直接靶向这些蛋白的潜力,特别是因为它们参与赋予对传统癌症疗法的抗性。还讨论了这种靶向策略的有效性,考虑到肿瘤对抗凋亡途径的倾向。此外,综述强调了联合疗法的新兴研究,其中BCL-2抑制剂与其他治疗协同使用以提高治疗效果。通过理解和操纵BCL-2家族及其相关途径,我们为创新和更有效的癌症治疗打开了大门,为耐药和侵袭性病例带来了希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b37/11063480/55ef6daae0f5/bt-32-3-267-f1.jpg

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