甲胎蛋白:一种革命性的抗癌药物

V. Pak
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摘要

甲胎蛋白是胚胎在胎儿发育过程中产生的一种癌胎蛋白。这种蛋白质同时具有两个关键功能:它向生长中的胚胎细胞和未成熟的髓源性抑制细胞提供营养,这样母亲的免疫系统就不会攻击胚胎。这种蛋白在成人中含量极低,升高的甲胎蛋白水平可以作为妊娠或肿瘤的标志。外源性甲胎蛋白作为免疫治疗药物具有新的应用前景。它能以自然穿梭的方式将药物输送到髓源性抑制细胞,并刺激它们来平息许多生理和病理条件下过度活跃的免疫反应。另一方面,携带毒素的甲胎蛋白杀死髓源性抑制细胞,释放自然杀伤细胞和细胞毒性淋巴细胞来清除癌症。大多数癌症都有与甲胎蛋白特异性结合的细胞,这种蛋白也针对它们进行化疗。因此,带毒素的甲胎蛋白结合了有效的癌症免疫治疗和靶向化疗活性。甲胎蛋白可以化学偶联或结合毒素非共价。与单独化疗相比,这两种制剂均显示出优越的疗效和安全性。甲胎蛋白毒素免疫/化疗不是个体化的。没有必要预先选择患者进行癌症治疗,因为他们有升高的髓源性抑制细胞水平。猪甲胎蛋白非共价复合物与选定毒素口服的抗癌功效是一个值得研究的重大发现。癌症的治疗和预防是不同的问题,它们可能需要不同的方法。甲胎蛋白与药物或毒素联合使用在预防早期癌症和转移方面可能与米非司酮预防妊娠一样有效。
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Alpha-Fetoprotein: A Revolutionary Anti-Cancer Drug
Alpha-fetoprotein is an oncofetal protein the embryo produces during fetal development. The protein serves two critical functions simultaneously: it delivers nutrients to growing embryo cells and immature myeloid-derived suppressor cells, so the mother’s immune system doesn’t attack the embryo. The protein is present in minuscule amounts in adults and elevated alpha-fetoprotein levels serve as pregnancy or tumor markers. Exogenous alpha-fetoprotein has a new application as an immunotherapy drug. It can deliver drugs in a natural shuttle manner to myeloid-derived suppressor cells and stimulate them to calm the hyperactive immune response during many physiological and pathological conditions. On the other hand, alpha-fetoprotein loaded with toxins kills myeloid-derived suppressor cells and unleashes natural killer cells and cytotoxic lymphocytes to erase cancer. Most cancers have cells that specifically bind alpha-fetoprotein, and this protein targets chemotherapy to them also. So, alpha-fetoprotein with toxins combines both potent cancer immunotherapy and targeted chemotherapy activities. Alpha-fetoprotein can be chemically conjugated with or bind toxins non-covalently. Both preparations have demonstrated superior efficacy and safety compared to chemotherapy alone. Alpha-fetoprotein-toxin immuno/chemotherapy is not personalized. There is no need to preselect patients for cancer treatments as they have elevated myeloid-derived suppressor cell levels. The anti-cancer efficacy of porcine alpha-fetoprotein non-covalent complexes with selected toxins administered orally is a remarkable discovery that needs research. Cancer treatment and prevention are different issues, and they could need different approaches. Alpha-fetoprotein administration with drugs or toxins could be as effective in early cancer and metastasis prevention as mifepristone pills in pregnancy prevention.
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