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癌症;一种二十世纪引发的疾病!耐受性的诱导、熵的增加与“暗能量”:生物节律的丧失(合成代谢对分解代谢)

Cancer; an induced disease of twentieth century! Induction of tolerance, increased entropy and 'Dark Energy': loss of biorhythms (Anabolism v. Catabolism).

作者信息

Khatami Mahin

机构信息

Inflammation, Aging and Cancer, National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, USA.

出版信息

Clin Transl Med. 2018 Jul 2;7(1):20. doi: 10.1186/s40169-018-0193-6.

Abstract

Maintenance of health involves a synchronized network of catabolic and anabolic signals among organs/tissues/cells that requires differential bioenergetics from mitochondria and glycolysis (biological laws or biorhythms). We defined biological circadian rhythms as Yin (tumoricidal) and Yang (tumorigenic) arms of acute inflammation (effective immunity) involving immune and non-immune systems. Role of pathogens in altering immunity and inducing diseases and cancer has been documented for over a century. However, in 1955s decision makers in cancer/medical establishment allowed public (current baby boomers) to consume million doses of virus-contaminated polio vaccines. The risk of cancer incidence and mortality sharply rose from 5% (rate of hereditary/genetic or innate disease) in 1900s, to its current scary status of 33% or 50% among women and men, respectively. Despite better hygiene, modern detection technologies and discovery of antibiotics, baby boomers and subsequent 2-3 generations are sicker than previous generations at same age. American health status ranks last among other developed nations while America invests highest amount of resources for healthcare. In this perspective we present evidence that cancer is an induced disease of twentieth century, facilitated by a great deception of cancer/medical establishment for huge corporate profits. Unlike popularized opinions that cancer is 100, 200 or 1000 diseases, we demonstrate that cancer is only one disease; the severe disturbances in biorhythms (differential bioenergetics) or loss of balance in Yin and Yang of effective immunity. Cancer projects that are promoted and funded by decision makers are reductionist approaches, wrong and unethical and resulted in loss of millions of precious lives and financial toxicity to society. Public vaccination with pathogen-specific vaccines (e.g., flu, hepatitis, HPV, meningitis, measles) weakens, not promotes, immunity. Results of irresponsible projects on cancer sciences or vaccines are increased population of drug-dependent sick society. Outcome failure rates of claimed 'targeted' drugs, 'precision' or 'personalized' medicine are 90% (± 5) for solid tumors. We demonstrate that aging, frequent exposures to environmental hazards, infections and pathogen-specific vaccines and ingredients are 'antigen overload' for immune system, skewing the Yin and Yang response profiles and leading to induction of 'mild', 'moderate' or 'severe' immune disorders. Induction of decoy or pattern recognition receptors (e.g., PRRs), such as IRAK-M or IL-1dRs ('designer' molecules) and associated genomic instability and over-expression of growth promoting factors (e.g., pyruvate kinases, mTOR and PI3Ks, histamine, PGE2, VEGF) could lead to immune tolerance, facilitating cancer cells to hijack anabolic machinery of immunity (Yang) for their increased growth requirements. Expression of constituent embryonic factors would negatively regulate differentiation of tumor cells through epithelial-mesenchymal-transition and create "dual negative feedback loop" that influence tissue metabolism under hypoxic conditions. It is further hypothesized that induction of tolerance creates 'dark energy' and increased entropy and temperature in cancer microenvironment allowing disorderly cancer proliferation and mitosis along with increased glucose metabolism via Crabtree and Pasteur Effects, under mitophagy and ribophagy, conditions that are toxic to host survival. Effective translational medicine into treatment requires systematic and logical studies of complex interactions of tumor cells with host environment that dictate clinical outcomes. Promoting effective immunity (biological circadian rhythms) are fundamental steps in correcting host differential bioenergetics and controlling cancer growth, preventing or delaying onset of diseases and maintaining public health. The author urges independent professionals and policy makers to take a closer look at cancer dilemma and stop the 'scientific/medical ponzi schemes' of a powerful group that control a drug-dependent sick society before all hopes for promoting public health evaporate.

摘要

健康的维持涉及器官/组织/细胞间分解代谢和合成代谢信号的同步网络,这需要线粒体和糖酵解产生不同的生物能量(生物规律或生物节律)。我们将生物昼夜节律定义为急性炎症(有效免疫)的阴(抗癌)和阳(致癌)两个方面,涉及免疫系统和非免疫系统。病原体在改变免疫力、诱发疾病和癌症方面的作用已有一个多世纪的记载。然而,在20世纪50年代,癌症/医疗机构的决策者允许公众(当前的婴儿潮一代)接种数百万剂受病毒污染的脊髓灰质炎疫苗。癌症发病率和死亡率的风险从20世纪初的5%(遗传性/基因性或先天性疾病的发病率)急剧上升到目前令人恐惧的水平,女性和男性分别为33%或50%。尽管卫生条件有所改善、现代检测技术不断发展且发现了抗生素,但婴儿潮一代以及随后的两三代人在相同年龄时比前几代人更易患病。美国的健康状况在其他发达国家中排名垫底,而美国在医疗保健方面投入的资源最多。从这个角度来看,我们提供证据表明癌症是20世纪的一种诱发疾病,是癌症/医疗机构为了巨额企业利润而进行的巨大欺骗行为所致。与普遍认为癌症是100种、200种或1000种疾病的观点不同,我们证明癌症只是一种疾病;是生物节律(不同的生物能量)受到严重干扰或有效免疫的阴阳失衡。由决策者推动和资助的癌症项目是还原论方法,是错误且不道德的,导致数百万宝贵生命丧失以及对社会造成经济毒性。用针对病原体的疫苗(如流感、肝炎、人乳头瘤病毒、脑膜炎、麻疹疫苗)进行公众接种会削弱而非增强免疫力。癌症科学或疫苗方面不负责任项目的结果是使药物依赖型患病社会的人口增加。对于实体瘤,所谓“靶向”药物、“精准”或“个性化”医学的声称疗效失败率为90%(±5)。我们证明衰老、频繁接触环境危害、感染以及针对病原体的疫苗和成分对免疫系统来说是“抗原过载”,使阴阳反应谱发生偏差,导致“轻度”“中度”或“重度”免疫紊乱的诱发。诱骗或模式识别受体(如IRAK - M或IL - 1dRs,“设计”分子)以及相关的基因组不稳定和生长促进因子(如丙酮酸激酶、mTOR和PI3K、组胺、PGE2、VEGF)的过度表达可能导致免疫耐受,促使癌细胞劫持免疫的合成代谢机制(阳)以满足其增加的生长需求。组成胚胎因子的表达会通过上皮 - 间质转化对肿瘤细胞的分化产生负调控,并形成“双负反馈回路”,在缺氧条件下影响组织代谢。进一步推测,耐受的诱导会在癌症微环境中产生“暗能量”并增加熵和温度,使癌症无序增殖和有丝分裂,同时通过克列勃屈利效应和巴斯德效应增加葡萄糖代谢,在细胞自噬和核糖体自噬的情况下,这些条件对宿主生存有毒性。有效的转化医学治疗需要对肿瘤细胞与宿主环境的复杂相互作用进行系统且合乎逻辑的研究,这些相互作用决定了临床结果。促进有效免疫(生物昼夜节律)是纠正宿主不同生物能量和控制癌症生长、预防或延迟疾病发作以及维持公众健康的基本步骤。作者敦促独立专业人士和政策制定者更仔细地审视癌症困境,在促进公众健康的所有希望破灭之前,停止控制药物依赖型患病社会的强大团体的“科学/医学庞氏骗局”。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9134/6026585/c5d0f0853d31/40169_2018_193_Fig1_HTML.jpg

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