Hyperglycosylated hCG Drives Malignancy in Most or All Human Cancers: Tying All Research Together

L. Cole
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引用次数: 5

Abstract

Objectives : Two forms of hCG are produced, the hormone hCG binding a luteinizing hormone/hCG joint receptor and the autocrine hyperglycosylated hCG binding a TGF-AŸ receptor. In pregnancy, hyperglycosylated hCG drives placental cell growth and invasion in implantation of pregnancy. It also blocks apoptosis. Human cancer cells steal the hCG AŸ-subunit gene and use hyperglycosylated hCG and its AŸ-subunit to drive malignancy. Here we examine research into hyperglycosylated hCG and its AŸ-subunit, and show that these molecules drive malignancy in most or possibly all human cancers. Methods : Mouse monoclonal antibody B152was raised against intact hyperglycosylated hCG, batch C5. The antibody binds hyperglycosylated hCG and its AŸ-subunit but does not bind the hormone hCG or its subunits. Total hCG was measured using the Siemens Immulite hCG assay, hyperglycosylated hCG and its AŸ-subunit were measured using the antibody B152 assay. Results : Eight independent center show that the hCG AŸ-subunit produced by cancers promotes malignancy, enhances cancer cell growth, cancer cell invasion and blockage of apoptosis in cancers. A study of 42 choriocarcinoma cases shows that percentage hyperglycosylated hCG exactly correlates with weekly doubling rate of cancer. It is concluded that hyperglycosylated hCG drive malignancy in this cancer. In a study with 7 separate cancers it is shown that increasing concentrations of hyperglycosylated hCG enhance all cancers. Increasing concentration of monoclonal antibody B152. Hyperglycosylated hCG and its AŸ-subunit drives cancer growth, cancer invasion and blocks apoptosis in cancer cells. Antibody B152 suppressed cancer cell growth creating a non-malignant-like state (no growth, no invasion), with no cancer growth over a starting 70% confluency. Conclusions : Choriocarcinoma is an example of cancer driven in malignancy by hyperglycosylated hCG, cancer aggression (weekly doubling rate) exactly correlating with percent hyperglycosylated hCG. In examining cancers, antibody B152 suppresses malignancy totally halting cancer growth in 7 of 7 cancer. This confirms that only the antigens, hyperglycosylated hCG and its AŸ-subunit drives malignancy in cancer cases.
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高糖基化hCG在大多数或所有人类癌症中驱动恶性肿瘤:将所有研究联系在一起
目的:产生两种形式的hCG,结合黄体生成素/hCG联合受体的激素hCG和结合TGF-AŸ受体的自分泌高糖基化hCG。在妊娠期间,高糖基化hCG在妊娠着床过程中驱动胎盘细胞的生长和侵袭。它还能阻止细胞凋亡。人类癌细胞窃取hCG AŸ-subunit基因,并利用高糖化hCG及其AŸ-subunit驱动恶性肿瘤。在这里,我们检查了对高糖基化hCG及其AŸ-subunit的研究,并表明这些分子在大多数或可能所有人类癌症中驱动恶性肿瘤。方法:制备小鼠单克隆抗体b152,抗完整高糖基化hCG,批次C5。抗体结合高糖基化hCG及其AŸ-subunit,但不结合激素hCG或其亚基。总hCG采用Siemens Immulite hCG法测定,高糖化hCG及其AŸ-subunit采用抗体B152法测定。结果:8个独立中心的研究表明,肿瘤产生的hCG AŸ-subunit促进肿瘤恶性,增强癌细胞生长,癌细胞侵袭,阻断肿瘤细胞凋亡。一项对42例绒毛膜癌病例的研究表明,高糖基化hCG的百分比与每周癌症加倍率完全相关。结论:高糖基化hCG驱动恶性肿瘤。一项针对7种不同癌症的研究表明,高糖基化hCG浓度的增加会加剧所有癌症。单克隆抗体B152浓度升高。高糖基化的hCG及其AŸ-subunit驱动癌细胞生长、侵袭和阻止癌细胞凋亡。抗体B152抑制癌细胞生长,产生非恶性样状态(无生长,无侵袭),初始合流率为70%以上,无肿瘤生长。结论:绒毛膜癌是由高糖基化hCG驱动的恶性肿瘤的一个例子,肿瘤侵袭性(每周加倍率)与高糖基化hCG的百分比完全相关。在检查癌症时,抗体B152抑制恶性肿瘤,完全阻止7种癌症的生长。这证实,只有抗原,高糖基化hCG及其AŸ-subunit驱动恶性肿瘤病例。
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