CA125/MUC16 Is Dispensable for Mouse Development and Reproduction

被引:30
作者
Cheon, Dong-Joo [1 ,2 ]
Wang, Ying [2 ]
Deng, Jian Min [2 ]
Lu, Zhen [3 ]
Xiao, Lianchun [4 ]
Chen, Chun-Ming [1 ]
Bast, Robert C., Jr. [3 ]
Behringer, Richard R. [1 ,2 ]
机构
[1] Univ Texas Houston, Grad Sch Biomed Sci, Program Genes & Dev, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Genet, Houston, TX USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX USA
关键词
D O I
10.1371/journal.pone.0004675
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Cancer antigen 125 (CA125) is a blood biomarker that is routinely used to monitor the progression of human epithelial ovarian cancer (EOC) and is encoded by MUC16, a member of the mucin gene family. The biological function of CA125/MUC16 and its potential role in EOC are poorly understood. Here we report the targeted disruption of the of the Muc16 gene in the mouse. To generate Muc16 knockout mice, 6.0 kb was deleted that included the majority of exon 3 and a portion of intron 3 and replaced with a lacZ reporter cassette. Loss of Muc16 protein expression suggests that Muc16 homozygous mutant mice are null mutants. Muc16 homozygous mutant mice are viable, fertile, and develop normally. Histological analysis shows that Muc16 homozygous mutant tissues are normal. By the age of 1 year, Muc16 homozygous mutant mice appear normal. Downregulation of transcripts from another mucin gene (Muc1) was detected in the Muc16 homozygous mutant uterus. Lack of any prominent abnormal phenotype in these Muc16 knockout mice suggests that CA125/MUC16 is not required for normal development or reproduction. These knockout mice provide a unique platform for future studies to identify the role of CA125/MUC16 in organ homeostasis and ovarian cancer.
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页数:8
相关论文
共 29 条
[1]
CA 125: The past and the future [J].
Bast, RC ;
Xu, FJ ;
Yu, YH ;
Barnhill, S ;
Zhang, Z ;
Mills, GB .
INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 1998, 13 (04) :179-187
[2]
Peritoneal natural killer cells from epithelial ovarian cancer patients show an altered phenotype and bind to the tumour marker MUC16 (CA125) [J].
Belisle, Jennifer A. ;
Gubbels, Jennifer A. A. ;
Raphael, Cara A. ;
Migneault, Martine ;
Rancourt, Claudine ;
Connor, Joseph P. ;
Patankar, Manish S. .
IMMUNOLOGY, 2007, 122 (03) :418-429
[3]
Functions of MUC16 in corneal epithelial cells [J].
Blalock, Timothy D. ;
Spurr-Michaud, Sandra J. ;
Tisdale, Ann S. ;
Heimer, Susan R. ;
Gilmore, Michael S. ;
Ramesh, Vijaya ;
Gipson, Ilene K. .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2007, 48 (10) :4509-4518
[4]
BRAGA VMM, 1993, J CELL SCI, V105, P397
[6]
MUC16 is produced in tracheal surface epithelium and submucosal glands and is present in secretions from normal human airway and cultured bronchial epithelial cells [J].
Davies, Julia R. ;
Kirkham, Sara ;
Svitacheva, Naila ;
Thornton, David J. ;
Carlstedt, Ingemar .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2007, 39 (10) :1943-1954
[7]
Gaetje R, 2002, Clin Exp Obstet Gynecol, V29, P34
[8]
Ovarian cancer antigen CA 125 enhances the invasiveness of the endometriotic cell line EEC 145 [J].
Gaetje, R ;
Winnekendonk, DW ;
Scharl, A ;
Kaufmann, M .
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 1999, 6 (05) :278-281
[9]
MUC16 is lost from the uterodome (pinopode) surface of the receptive human endometrium: In vitro evidence that MUC16 is a barrier to trophoblast adherence [J].
Gipson, Ilene K. ;
Blalock, Timothy ;
Tisdale, Ann ;
Spurr-Michaud, Sandra ;
Allcorn, Sara ;
Stavreus-Evers, Anneli ;
Gemzell, Kristina .
BIOLOGY OF REPRODUCTION, 2008, 78 (01) :134-142
[10]
DISTRIBUTION OF CA125 IN EMBRYONIC-TISSUES AND ADULT DERIVATIVES OF THE FETAL PERIDERM [J].
HARDARDOTTIR, H ;
PARMLEY, TH ;
QUIRK, JG ;
SANDERS, MM ;
MILLER, FC ;
OBRIEN, TJ .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1990, 163 (06) :1925-1931