Cell reprogramming in cancer: Interplay of genetic, epigenetic mechanisms, and the tumor microenvironment in carcinogenesis and metastasis.

IF 3.2 Q3 ONCOLOGY
Santosh Shenoy
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Abstract

Cell plasticity, also known as lineage plasticity, refers to the ability of a cell to reprogram and change its phenotypic identity in response to various cues. This phenomenon is context-dependent, playing a crucial role in embryonic development, tissue regeneration, and wound healing. However, when dysregulated, cell plasticity contributes to cancer initiation, progression, metastasis, and therapeutic resistance. Throughout different stages of tumor development, cancer cells exploit various forms of plasticity to evade normal regulatory mechanisms that govern cell division and homeostasis. Recent evidence highlights the complex interplay between genetic and epigenetic factors, the tumor microenvironment, and epithelial-to-mesenchymal transition in driving cancer cell plasticity. This dynamic reprogramming suggests that "deregulated cell plasticity" could be considered an additional hallmark of cancer. Advancements in next-generation sequencing and single-cell RNA analysis, combined with artificial intelligence technologies such as deep learning, along with Google's AlphaFold may help predict the trajectories of cancer cells. By predicting protein three-dimensional structures and identifying both active and potential allosteric binding sites, AlphaFold 2 can accelerate the development of new cancer drugs and therapies. For example, allosteric drugs, bind to the allosteric rather than the active sites, can induce conformational changes in proteins, affecting their activities. This can then alter the conformation of an active site that a drug-resistant mutation has created, permitting a blocked orthosteric drug to bind and this enables the design of more effective drugs that can synergize with traditional orthosteric drugs to bind and regain its efficacy. These innovations could provide deeper insights into the intricate mechanisms of cancer progression and resistance, ultimately paving the way for more precise, durable, and personalized oncologic treatments.

Abstract Image

癌症中的细胞重编程:遗传、表观遗传机制和肿瘤微环境在癌变和转移中的相互作用。
细胞可塑性,也被称为谱系可塑性,是指细胞在响应各种线索时重编程和改变其表型身份的能力。这种现象与环境有关,在胚胎发育、组织再生和伤口愈合中起着至关重要的作用。然而,当失调时,细胞可塑性有助于癌症的发生、进展、转移和治疗耐药性。在肿瘤发展的不同阶段,癌细胞利用各种形式的可塑性来逃避控制细胞分裂和稳态的正常调节机制。最近的证据强调了遗传和表观遗传因素、肿瘤微环境和上皮-间质转化之间复杂的相互作用在驱动癌细胞可塑性。这种动态重编程表明,“不受控制的细胞可塑性”可能被认为是癌症的另一个标志。下一代测序和单细胞RNA分析的进步,结合深度学习等人工智能技术,以及谷歌的AlphaFold,可能有助于预测癌细胞的轨迹。通过预测蛋白质三维结构和识别活性和潜在的变构结合位点,AlphaFold 2可以加速新的癌症药物和治疗方法的开发。例如,变构药物,结合到变构位点而不是活性位点,可以诱导蛋白质的构象变化,影响其活性。然后,这可以改变耐药突变产生的活性位点的构象,允许被阻断的正畸药物结合,这使得设计更有效的药物能够与传统的正畸药物协同作用,结合并恢复其功效。这些创新可以为癌症进展和耐药性的复杂机制提供更深入的见解,最终为更精确、持久和个性化的肿瘤治疗铺平道路。
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来源期刊
自引率
0.00%
发文量
585
期刊介绍: The WJCO is a high-quality, peer reviewed, open-access journal. The primary task of WJCO is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of oncology. In order to promote productive academic communication, the peer review process for the WJCO is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJCO are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in oncology. Scope: Art of Oncology, Biology of Neoplasia, Breast Cancer, Cancer Prevention and Control, Cancer-Related Complications, Diagnosis in Oncology, Gastrointestinal Cancer, Genetic Testing For Cancer, Gynecologic Cancer, Head and Neck Cancer, Hematologic Malignancy, Lung Cancer, Melanoma, Molecular Oncology, Neurooncology, Palliative and Supportive Care, Pediatric Oncology, Surgical Oncology, Translational Oncology, and Urologic Oncology.
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