Cole Laurence A, Dai Donghai, Butler Stephen A, Leslie Kimberly K, Kohorn Ernest I
Department of Obstetrics and Gynecology, MSC10 5580 1 University of New Mexico, Albuquerque, NM 87131-0001, USA.
Gynecol Oncol. 2006 Aug;102(2):145-50. doi: 10.1016/j.ygyno.2005.12.047. Epub 2006 May 2.
Hyperglycosylated hCG (hCG-H) is a glycosylation variant of hCG produced by cytotrophoblast cells at implantation of pregnancy and in choriocarcinoma. We investigated the biological function of hCG-H in invasion in vitro and in vivo and the use of hCG-H antibodies in blocking tumorigenesis and cancer growth in vivo.
hCG-H accounts for 43% to 100% of total hCG immunoreactivity in the culture fluid of choriocarcinoma cell lines and 100% in primary cultures of pregnancy cytotrophoblast cells. We investigated the action of hCG and hCG-H on isolated cytotrophoblast cell primary cultures and on 3 different lines of choriocarcinoma cells cultured on Matrigel basement membrane inserts (culture models for assessing tumor invasion). The addition of hCG-H to medium significantly promoted invasion of membranes with both pregnancy and cancer cell line sources, while regular hCG had no significant effect. JEG-3 human choriocarcinoma cells were transplanted subcutaneously into athymic nude mice. Tumors rapidly formed. B152, mouse monoclonal antibody against hCG-H, and non-specific mouse IgG (control) were administered twice weekly once tumors were clearly visible. While a correlation between time and growth was observed with the control group (r(2)=0.97), no correlation was observed with the B152-treated mice (r(2)=0.15). B152 blocked tumor growth (t test, IgG vs. B152, P=0.003). In a second experiment, antibody B152 or IgG was administered to mice at the time of choriocarcinoma transplantation. B152 significantly inhibited tumorigenesis (t test P=0.0071).
hCG-H is a critical promoter in human cytotrophoblast and human choriocarcinoma cell invasion in vivo and in vitro, promoting tumor growth and invasion through an autocrine mechanism. hCG-H is a signal for choriocarcinoma cell invasion, making it a biological tumor marker. Antibodies against hCG-H block tumor formation and growth. Human or humanized antibodies against hCG-H may be useful in treating and managing choriocarcinoma and other gestational trophoblastic malignancies.
高糖基化人绒毛膜促性腺激素(hCG-H)是妊娠着床时细胞滋养层细胞以及绒毛膜癌中产生的hCG的一种糖基化变体。我们研究了hCG-H在体外和体内侵袭中的生物学功能,以及hCG-H抗体在体内阻断肿瘤发生和癌症生长方面的作用。
在绒毛膜癌细胞系培养液中,hCG-H占总hCG免疫反应性的43%至100%,在妊娠细胞滋养层细胞原代培养物中占100%。我们研究了hCG和hCG-H对分离的细胞滋养层细胞原代培养物以及在基质胶基底膜小室上培养的3种不同绒毛膜癌细胞系(用于评估肿瘤侵袭的培养模型)的作用。向培养基中添加hCG-H显著促进了来自妊娠和癌细胞系来源的细胞对膜的侵袭,而常规hCG则无显著影响。将JEG-3人绒毛膜癌细胞皮下移植到无胸腺裸鼠体内。肿瘤迅速形成。一旦肿瘤清晰可见,每周两次给予抗hCG-H的小鼠单克隆抗体B152和非特异性小鼠IgG(对照)。虽然在对照组中观察到时间与生长之间的相关性(r² = 0.97),但在接受B152治疗的小鼠中未观察到相关性(r² = 0.15)。B152阻断了肿瘤生长(t检验,IgG与B152相比,P = 0.003)。在第二个实验中,在绒毛膜癌移植时给小鼠注射抗体B15或者IgG。B152显著抑制了肿瘤发生(t检验,P = 0.0071)。
hCG-H是体内外人类细胞滋养层细胞和人绒毛膜癌细胞侵袭的关键促进因子,通过自分泌机制促进肿瘤生长和侵袭。hCG-H是绒毛膜癌细胞侵袭的信号,使其成为一种生物学肿瘤标志物。抗hCG-H抗体可阻断肿瘤形成和生长。针对hCG-H的人源或人源化抗体可能有助于治疗和管理绒毛膜癌及其他妊娠滋养层恶性肿瘤。