32βhCG down-regulates E-Cadherin and thus promotes migration and

32βhCG down-regulates E-Cadherin and thus promotes migration and invasion of cancer cells.33 Evidences indicate that the sudden transformation of non-trophoblastic benign tumors to the malignant type can be attributed to altered genetic expression of βhCG. Benign non-trophoblastic cancer cells expressing type I CG β genes (β6 and β7), which transcribe βhCG with an alanine residue at the position 117, start expressing type II CG β genes (β8,β5,β3,β9) that transcribe

βhCG with aspartate residue at position 117 during malignant transformation.34 A possible molecular mechanism by which hCG can promote neoplasm has been proposed recently, which suggests that hCG up-regulates the cell cycle proteins via the mammalian target Maraviroc datasheet of rapamycin complex 1 (mTORC1) signaling network.35 Thus, hCG is involved not only in the onset, progression, and maintenance of pregnancy but also in cancers. Recent observations show the presence of hCG or its subunits in a variety of advanced-stage cancers invariably metastasized, radio-resistant, and refractory to available drugs. Vaccines against cancer are therefore expected to have a dual utility of not only in preventing an unwanted pregnancy but also in therapy of hitherto untreatable terminal cancers expressing ectopically hCG or its subunits.

Immunological inactivation of hCG can be achieved by both active (vaccination) and passive immunization (use of preformed competent antibodies). Vaccination produces a long-term response, whereas the passive immunization is of finite duration. Preformed antibodies R788 in vitro offer a mode of ready intervention. There is no lag period of action, in contrast to the time period required for generation and build up of antibodies following first time vaccination. Efficacy tuclazepam is assured in all recipients over a finite period based on the biological half-life of about 21 days of humanized/chimeric antibodies in humans. On the other hand, the duration of the antibody response after vaccination

varies from individual to individual as also the quantum of antibodies formed. Thus, efficacy cannot be guaranteed in all recipients unless the vaccine produces above protective threshold response in all. The following applications are feasible by employing anti-hCG antibodies: hCG plays a critical role in implantation of the embryo, which is believed to take place between 6th and 9th day following ovulation in women. Antibodies competent to inactivate hCG bioactivity intercept implantation, hence prevent the onset of pregnancy.3,4 At present, Levo-Norgesterol is employed for emergency contraception, which has to be taken within 48–72 hr of unprotected sex. This window of emergency contraception can be extended by some precious days by taking anti-hCG antibodies.

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