TY - JOUR
T1 - Nonobese diabetic/severe combined immunodeficient murine xenograft model for human uterine leiomyoma
AU - Wang, Guiwen
AU - Ishikawa, Hiroshi
AU - Sone, Kunizui
AU - Kobayashi, Tatsuya
AU - Kim, J. Julie
AU - Kurita, Takeshi
AU - Shozu, Makio
PY - 2014/5
Y1 - 2014/5
N2 - Objective To establish a novel xenograft model using a severely immunocompromised host that is more convenient for uterine leiomyoma research compared with a pre-existing model using nonobese diabetic/severe combined immunodeficient (NOD/SCID) IL-2Rγ-null mice. Design Experimental study. Setting University and an attached animal facility. Animal(s) NOD/SCID, SCID, BALB/c nude, and NOD/SCID IL-2Rγ-null mice. Intervention(s) Xenografts consisting of primary cultured leiomyoma and myometrial cells in the subrenal and subcutaneous (SC) spaces in ovariectomized mice, followed by sex steroids (estrogen and P) administration. Main Outcome Measure(s) Viability, volume, histology, and sex steroid receptor expression of xenografts in response to sex steroid administration, to evaluate feasibility of the model; and messenger RNA expression levels of 12 genes representative of leiomyoma in the xenografts, to characterize the model. Result(s) Leiomyoma xenografts increased in volume at the highest frequency (55.1%) in response to sex steroids in NOD/SCID mice. Xenografts reproduced the histology and maintained expression of sex steroids receptors and representative genes of the original tissues. Subrenal xenografts were significantly larger than the SC xenografts, whereas those consisting of myometrial cells never increased. Conclusion(s) The modified NOD/SCID murine subrenal leiomyoma xenograft model reproduced most characteristics of the original leiomyoma tissue. Our model provides a more convenient research tool to investigate the pathogenesis of uterine leiomyoma.
AB - Objective To establish a novel xenograft model using a severely immunocompromised host that is more convenient for uterine leiomyoma research compared with a pre-existing model using nonobese diabetic/severe combined immunodeficient (NOD/SCID) IL-2Rγ-null mice. Design Experimental study. Setting University and an attached animal facility. Animal(s) NOD/SCID, SCID, BALB/c nude, and NOD/SCID IL-2Rγ-null mice. Intervention(s) Xenografts consisting of primary cultured leiomyoma and myometrial cells in the subrenal and subcutaneous (SC) spaces in ovariectomized mice, followed by sex steroids (estrogen and P) administration. Main Outcome Measure(s) Viability, volume, histology, and sex steroid receptor expression of xenografts in response to sex steroid administration, to evaluate feasibility of the model; and messenger RNA expression levels of 12 genes representative of leiomyoma in the xenografts, to characterize the model. Result(s) Leiomyoma xenografts increased in volume at the highest frequency (55.1%) in response to sex steroids in NOD/SCID mice. Xenografts reproduced the histology and maintained expression of sex steroids receptors and representative genes of the original tissues. Subrenal xenografts were significantly larger than the SC xenografts, whereas those consisting of myometrial cells never increased. Conclusion(s) The modified NOD/SCID murine subrenal leiomyoma xenograft model reproduced most characteristics of the original leiomyoma tissue. Our model provides a more convenient research tool to investigate the pathogenesis of uterine leiomyoma.
KW - Leiomyoma
KW - NOD/SCID
KW - animal model
KW - xenograft
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U2 - 10.1016/j.fertnstert.2014.01.054
DO - 10.1016/j.fertnstert.2014.01.054
M3 - Article
C2 - 24636398
AN - SCOPUS:84899914254
SN - 0015-0282
VL - 101
SP - 1485-1492.e3
JO - Fertility and Sterility
JF - Fertility and Sterility
IS - 5
ER -