催产素抗癌特性的初步研究:联合催产素、抗肿瘤松果体吲哚和大麻二酚治疗仅靠松果体吲哚和大麻二酚治疗的晚期癌症患者的神经内分泌方案

Oncogen Pub Date : 2019-09-27 DOI:10.35702/onc.10018
P. Lissoni, G. Porro, F. Rovelli, G. Messina, Rosa Cusmai, Alberto Caddeo, R. Trampetti, E. Porta, A. Monzon, M. Roselli, G. Di Fede
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In fact, cancer progression has appeared to be associated with a progressive decline in the functionless of the pineal gland and endocannabinoid system. The endocannabinoid brain activity may be enhanced by the non-psychoactive principle A Preliminary Study on the Anticancer Properties of Oxytocin: A Neuroendocrine Regimen with Oxytocin, Antitumor Pineal Indoles, and Cannabidiol in Untreatable Advanced Cancer Patients Progressing on Pineal Indoles and Cannabidiol Alone. Oncogen 2(4): 18. system [9] and probably to a dimished OXY secretion [13]. Then, the progressive correction of these major cancer-related neuroendocrine deficiencies through an exogenous administration could improve the control of cancer growth. 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引用次数: 0

摘要

最近发现了几种内源性和外源性抗癌无毒分子,这使得对那些通常被认为有资格接受姑息治疗的患者实施潜在的抗癌治疗方案成为可能。在人体的抗癌分子中,松果体吲哚激素和内源性大麻素药物可能通过多种机制对大多数肿瘤组织型发挥抗癌活性,包括对肿瘤免疫的细胞毒性、抗血管生成和免疫刺激作用,并延长晚期癌症患者唯一支持治疗的生存时间。事实上,癌症的进展似乎与松果体和内源性大麻素系统功能的逐渐下降有关。后叶催产素抗癌特性的初步研究:后叶催产素、抗肿瘤松果体吲哚和大麻二酚联合治疗仅靠松果体吲哚和大麻二酚治疗的晚期癌症患者的神经内分泌治疗方案致癌因子2(4):18。系统[9]和可能减少氧分泌[13]。因此,通过外源性给药逐步纠正这些主要的与癌症相关的神经内分泌缺陷可以改善对癌症生长的控制。事实上,一些初步的临床研究已经证明,通过给予大剂量松果体吲哚激素MLT和5-MTT[17],可以提高相当数量的晚期癌症患者的生存时间,即使在非常低比例的无法治疗的播散性癌症患者中,也可以实现一些肿瘤消退。进一步的研究表明,在黑暗期口服100 mg/天,在光明期口服10 mg/天,可能会更大程度地延长无法治疗的(5-MTT)的生存时间。CBD也给予口服,10毫克,2次/天。最后,以胃保护形式口服羟考酮2毫克/天2次。8/14(57%)例患者(妇科肿瘤:5例;TNBC: 2;GBM: 1),而6例患者为进行性疾病(PD)。SD患者的1年生存率明显高于PD患者。此外,9/14(64%)患者在服用羟色胺后情绪、社会关系和愉悦感均有明显改善。这些初步结果将进一步证实,通过简单纠正主要的癌症进展相关的内源性神经内分泌缺陷(包括松果体系统和OXY分泌),晚期癌症患者也有可能获得肿瘤生长控制。
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A Preliminary Study On The Anticancer Properties Of Oxytocin: A Neuroendocrine Regimen With Oxytocin, Antitumor Pineal Indoles, And Cannabidiol In Untreatable Advanced Cancer Patients Progressing On Pineal Indoles And Cannabidiol Alone
The recent discovery of several endogenous and exogenous anticancer non-toxic molecules has allowed the possibility to administer potential anticancer curative regimens also in patients, who would be generally considered as eligible for the only palliative therapy. Within the anticancer molecules of the human body, it has been shown that the pineal indole hormones and the endocannabinoid agents may play an anticancer activity against most tumor histotypes through several mechanisms, including cytotoxic, anti-angiogenic and immunostimulatory effect on the anticancer immunity, and to prolong the survival time in advanced cancer patients eligible for the only supportive care. In fact, cancer progression has appeared to be associated with a progressive decline in the functionless of the pineal gland and endocannabinoid system. The endocannabinoid brain activity may be enhanced by the non-psychoactive principle A Preliminary Study on the Anticancer Properties of Oxytocin: A Neuroendocrine Regimen with Oxytocin, Antitumor Pineal Indoles, and Cannabidiol in Untreatable Advanced Cancer Patients Progressing on Pineal Indoles and Cannabidiol Alone. Oncogen 2(4): 18. system [9] and probably to a dimished OXY secretion [13]. Then, the progressive correction of these major cancer-related neuroendocrine deficiencies through an exogenous administration could improve the control of cancer growth. In fact, some preliminary clinical studies have already demonstrated the possibility to enhance the survival time in a considerable number of advanced cancer patients eligible for the only palliative therapy, and also to achieve some tumor regressions even though in a very low percentage of untreatable disseminated cancer patients, through the administration of high-dose pineal indole hormones MLT and 5-MTT [17]. Further studies have shown the possibility to achieve a greater increase in the survival time of untreatable (5-MTT) were given orally at 100 mg/day in the dark period, and at 10 mg/day in the light period, respectively. CBD was also given orally at 10 mg twice/day. Finally, OXY was given orally at 2 mg twice/day in a gastroprotected form. A stable disease (SD) was achieved in 8/14 (57%) patients (gynecologic tumors: 5; TNBC: 2; GBM: 1), whereas 6 patients had a progressive disease (PD). The percentage of 1-year survival obtained in patients with SD was significantly higher than that found in patients with PD. Moreover, a clear improvement in mood, social relationships and pleasure perception was observed in 9/14 (64%) patients under OXY administration. These preliminary results would furtherly confirm the possibility to obtain a control of the neoplastic growth also in advanced cancer patients eligible for the only supportive care alone by simply correcting the main cancer- progression-related endogenous neuroendocrine deficiencies, including pineal system and OXY secretion.
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