Localization of telomerase hTERT protein and survivin in placenta: Relation to placental development and hydatidiform mole

被引:43
作者
Lehner, R
Bobak, J
Kim, NW
Shroyer, AL
Shroyer, KR
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Pathol, Denver, CO 80262 USA
[2] Geron Corp, Menlo Park, CA USA
[3] Vet Affairs Med Ctr, VA Div Cardiac Res, Denver, CO USA
关键词
D O I
10.1016/S0029-7844(01)01131-0
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To find if a difference in telomerase or survivin expression exists between non-neoplastic tissues and hydatidiform moles, and explore expression of those proteins in normal placental development, post-term gestation, and preeclampsia. Methods: Formalin-fixed placental tissues were selected from collections of the Department of Pathology at the University of Colorado. Five specimens of each trimester, five each of preeclamptic and post-term placentas, and 23 molar pregnancies were selected. The telomerase catalytic protein hTERT was localized in placental tissues using the catalyzed signal amplification system, and survivin was localized by conventional immunoperoxidase method. Staining was graded on a scale of zero to 4. Results: hTERT staining was detected in sections of 42 of 48 specimens (23 of 23 hydatidiform moles, 19 of 25 nonneoplastic placental tissues). The intensity of staining for hTERT was higher in hydatidiform moles (mean 3.3, median 3) compared with levels in non-neoplastic placental tissues (mean 0.92, median 1) (P <.001). Survivin was detected in 39 of 48 specimens (22 of 23 hydatidiform moles, 17 of 25 non-neoplastic placental tissues). Compared with nonneoplastic tissues (mean 0.88, median 1), survivin levels were elevated in hydatidiform moles (mean 1.35, median 1) (P =.031). Conclusion: Survivin and telomerase were increased in hydatidiform moles, suggesting that regulation of apoptosis and stabilization of telomere length might be involved in neoplastic transformation of the placenta. The patterns of expression observed for survivin and telomerase in nonneoplastic placental tissues suggest that the control of apoptosis and stabilization of telomeric DNA might also be involved in normal gestational development. (Obstet Gynecol 2001;97:965-70. (C) 2001 by The American College of Obstetricians and Gynecologists.).
引用
收藏
页码:965 / 970
页数:6
相关论文
共 26 条
[1]   Telomerase activity in germ cell cancers and mature teratomas [J].
Albanell, J ;
Bosl, GJ ;
Reuter, VE ;
Engelhardt, M ;
Franco, S ;
Moore, MAS ;
Dmitrovsky, E .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (15) :1321-1326
[2]   A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma [J].
Ambrosini, G ;
Adida, C ;
Altieri, DC .
NATURE MEDICINE, 1997, 3 (08) :917-921
[3]   STRUCTURE AND FUNCTION OF TELOMERES [J].
BLACKBURN, EH .
NATURE, 1991, 350 (6319) :569-573
[4]   Extension of life-span by introduction of telomerase into normal human cells [J].
Bodnar, AG ;
Ouellette, M ;
Frolkis, M ;
Holt, SE ;
Chiu, CP ;
Morin, GB ;
Harley, CB ;
Shay, JW ;
Lichtsteiner, S ;
Wright, WE .
SCIENCE, 1998, 279 (5349) :349-352
[5]   Apoptotic and proliferative activities in first trimester placentae [J].
Chan, CCW ;
Lao, TT ;
Cheung, ANY .
PLACENTA, 1999, 20 (2-3) :223-227
[6]   Telomerase activity is restored in human cells by ectopic expression of hTERT (hEST2), the catalytic subunit of telomerase [J].
Counter, CM ;
Meyerson, M ;
Eaton, EN ;
Ellisen, LW ;
Caddle, SD ;
Haber, DA ;
Weinberg, RA .
ONCOGENE, 1998, 16 (09) :1217-1222
[7]   THE RNA COMPONENT OF HUMAN TELOMERASE [J].
FENG, JL ;
FUNK, WD ;
WANG, SS ;
WEINRICH, SL ;
AVILION, AA ;
CHIU, CP ;
ADAMS, RR ;
CHANG, E ;
ALLSOPP, RC ;
YU, JH ;
LE, SY ;
WEST, MD ;
HARLEY, CB ;
ANDREWS, WH ;
GREIDER, CW ;
VILLEPONTEAU, B .
SCIENCE, 1995, 269 (5228) :1236-1241
[8]   Localization of telomerase hTERT protein and hTR in benign mucosa, dysplasia, and squamous cell carcinoma of the cervix [J].
Frost, M ;
Bobak, JB ;
Gianani, R ;
Kim, N ;
Weinrich, S ;
Spalding, DC ;
Cass, LG ;
Thompson, LC ;
Enomoto, T ;
Uribe-Lopez, D ;
Shroyer, KR .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2000, 114 (05) :726-734
[9]   Expression of survivin in normal, hyperplastic, and neoplastic colonic mucosa [J].
Gianani, R ;
Jarboe, E ;
Orlicky, D ;
Frost, M ;
Bobak, J ;
Lehner, R ;
Shroyer, KR .
HUMAN PATHOLOGY, 2001, 32 (01) :119-125
[10]  
Holt SE, 1999, MOL CARCINOGEN, V25, P241, DOI 10.1002/(SICI)1098-2744(199908)25:4<241::AID-MC2>3.3.CO