TY - JOUR
T1 - Differences between white and Chinese populations in human leukocyte antigen sharing and gestational trophoblastic tumors
AU - Ho, Hong Nerng
AU - Gill, Thomas J.
AU - Klionsky, Bernard
AU - Ouyang, Pei Chuan
AU - Hsieh, Chang Yao
AU - Seski, Jan
AU - Kunschner, Alan
PY - 1989/1/1
Y1 - 1989/1/1
N2 - The prevalence of gestational trophoblastic tumors varies widely among different populations: it is lowest in whites (3 to 6 100,000) and highest in Chinese (68 to 202 100,000). This observation suggests that the origin of the disease is different in the two populations. To test this hypothesis, we examined couples in whom the woman developed a gestational trophoblastic tumor in a white population (Pittsburgh) and a Chinese population (Taiwan) for sharing of human leukocyte A, B, DR, and DQ antigens, which we consider markers for sharing of major histocompatibility complex-linked recessive genes affecting both embryogenesis and carcinogenesis. No human leukocyte antigen sharing occurred between partners in Pittsburgh, but there was significant human leukocyte antigen sharing in Taiwan. The latter couples shared human leukocyte antigen B (p < 0.04) and human leukocyte antigen DQ (p < 0.007) and shared three or more human leukocyte A, B, DR, and DQ antigens (p < 0.02) significantly more frequently than did normal coupies. However, there was no increased sharing of any specific human leukocyte antigen allele. These findings support the hypothesis that gestational trophoblastic tumors occur on a sporadic basis in whites and on a genetic basis in Chinese.
AB - The prevalence of gestational trophoblastic tumors varies widely among different populations: it is lowest in whites (3 to 6 100,000) and highest in Chinese (68 to 202 100,000). This observation suggests that the origin of the disease is different in the two populations. To test this hypothesis, we examined couples in whom the woman developed a gestational trophoblastic tumor in a white population (Pittsburgh) and a Chinese population (Taiwan) for sharing of human leukocyte A, B, DR, and DQ antigens, which we consider markers for sharing of major histocompatibility complex-linked recessive genes affecting both embryogenesis and carcinogenesis. No human leukocyte antigen sharing occurred between partners in Pittsburgh, but there was significant human leukocyte antigen sharing in Taiwan. The latter couples shared human leukocyte antigen B (p < 0.04) and human leukocyte antigen DQ (p < 0.007) and shared three or more human leukocyte A, B, DR, and DQ antigens (p < 0.02) significantly more frequently than did normal coupies. However, there was no increased sharing of any specific human leukocyte antigen allele. These findings support the hypothesis that gestational trophoblastic tumors occur on a sporadic basis in whites and on a genetic basis in Chinese.
KW - choriocarcinoma
KW - genetics of cancer
KW - Gestational trophoblastic tumors
KW - human leukocyte antigen sharing
UR - http://www.scopus.com/inward/record.url?scp=0024446282&partnerID=8YFLogxK
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U2 - 10.1016/0002-9378(89)90758-8
DO - 10.1016/0002-9378(89)90758-8
M3 - Article
C2 - 2552808
AN - SCOPUS:0024446282
SN - 0002-9378
VL - 161
SP - 942
EP - 948
JO - American Journal of Obstetrics and Gynecology
JF - American Journal of Obstetrics and Gynecology
IS - 4
ER -