Synopsis: Special Issue on “Disruption of signaling homeostasis induced crosstalk in the carcinogenesis paradigm Epistemology of the origin of cancer”

4open Pub Date : 2019-01-01 DOI:10.1051/fopen/2019023
B. Brücher, I. Jamall
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引用次数: 3

Abstract

It is increasingly evident that carcinogenesis, in the vast majority of cancers, cannot be explained simply through an accumulation of somatic mutations, or epigenetics, the stem cell theory, or the Warburg effect. Here, decades of thinking based on incorrect assumptions has resulted in an incorrect hypothesis on the origin of cancer. Many papers studying DNA, genetics, RNA, miRNA, proteomics, and epigenetics have increased our understanding of biology. Our paradigm, though more complex, is more reliable and plausible. It states that cancer originates from a disruption of homeostasis. This essential biological phenomenon, homeostasis, maintains the interrelationships of various signaling pathways and induced crosstalk which modify cellular functions together with the interactions of surrounding cells and structures such that the equilibrium lies towards the optimal health of the organism. This Special Issue “Disruption of signaling homeostasis induced crosstalk in the carcinogenesis paradigm Epistemology of the origin of cancer” provides compelling evidence that carcinogenesis is explained by a six-step sequence of events for the vast majority of cancers. These six steps include, (1) a pathogenic stimulus followed by (2) chronic inflammation, from which develops (3) fibrosis with associated remodeling in the cellular microenvironment. From these changes a (4) pre-cancerous niche develops which triggers the deployment of (5) a chronic stress escape strategy, and when this fails to resolve, and (6) the transition of a normal cell to a cancer cell occurs. This paradigm provides opportunities to move away from a symptom-oriented understanding of cancer and is much closer to a cause-based understanding, which opens the door for early preventative strategies to mitigate cancer as a disease, and to interdict metastases. This is underpinned by the fact that an independent recently published proof of this paradigm showed how a stimulus trigger the proposed multi-sequence cascade of events as abrupt involution-induced chronic inflammation, followed by fibrosis with remodeling, which describes the pre-cancerous niche followed by hyperplasia, metaplasia, and cancer.
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摘要:特刊《癌变范式中信号稳态破坏引起的串扰:癌症起源认识论》
越来越明显的是,在绝大多数癌症中,癌变不能简单地通过体细胞突变的积累、表观遗传学、干细胞理论或沃伯格效应来解释。在这里,几十年来基于错误假设的思考导致了对癌症起源的错误假设。许多研究DNA、遗传学、RNA、miRNA、蛋白质组学和表观遗传学的论文增加了我们对生物学的理解。我们的范式虽然更复杂,但更可靠、更可信。它指出癌症起源于体内平衡的破坏。这种基本的生物现象,即体内平衡,维持各种信号通路的相互关系和诱导的串扰,这些串扰与周围细胞和结构的相互作用一起改变细胞功能,从而使平衡处于生物体的最佳健康状态。本期特刊《癌变范式的认识论中信号稳态的破坏引起的串扰》提供了令人信服的证据,证明绝大多数癌症的癌变可以用六个步骤的事件序列来解释。这六个步骤包括:(1)病原性刺激,随后(2)慢性炎症,由此发展(3)细胞微环境中纤维化和相关的重塑。从这些变化中,(4)癌前生态位形成,触发(5)慢性应激逃逸策略的部署,当这种策略无法解决时,(6)正常细胞向癌细胞的转变就发生了。这种模式提供了摆脱以症状为导向的癌症理解的机会,更接近于以原因为基础的理解,这为早期预防策略打开了大门,以减轻癌症作为一种疾病,并阻止转移。最近发表的一项独立研究证明了这一观点,该研究表明,刺激如何引发了一系列的连锁反应,如突然的渐开式慢性炎症,随后是纤维化和重塑,这描述了癌前生态位,随后是增生、化生和癌症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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