Gan Qiong, Crumley Suzanne, Broaddus Russell R
Department of Pathology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Int J Gynecol Pathol. 2019 Jan;38(1):44-51. doi: 10.1097/PGP.0000000000000465.
Endometrial endometrioid carcinoma is related to estrogen excess and expression of estrogen and progesterone receptors. Epidemiological evidence suggests that exposure to elevated androgens, as in polycystic ovarian syndrome, increases the risk of endometrial cancer. Factors impacting androgen receptor (AR) expression are not well studied. Mismatch repair (MMR) deficiency due to MLH1 gene methylation is one of the most common molecular alterations in endometrial cancer, occurring in 15% to 20% of cases. MLH1 methylation can be associated with decreased expression of other genes, so we examined the effect of MMR status on AR expression. As NF-κB is known to induce AR, this transcription factor was also examined. Three hundred forty-four unselected endometrial carcinomas were evaluated for DNA MMR. Loss of expression of MLH1 with MLH1 methylation was defined as MMR deficient, and positive expression of MMR proteins was defined as MMR intact. A case-control cohort of 96 grade 2 endometrioid carcinomas was studied from this set (47 MMR deficient, 49 MMR intact). Cases were matched for histotype, grade, and age. AR and NF-κB immunohistochemical expression were evaluated by 2 different scoring systems (CAP/ASCO and Allred) used for estrogen receptor. Despite higher levels of NF-κB, MMR deficiency was associated with a significantly lower mean percentage of AR expression. The MMR deficient group had more variable AR expression, with more cases scoring on the lower end of the spectrum. These findings have implications for clinical trials of AR antagonists in gynecologic cancers.
子宫内膜样腺癌与雌激素过量以及雌激素和孕激素受体的表达有关。流行病学证据表明,如多囊卵巢综合征中那样暴露于升高的雄激素会增加子宫内膜癌的风险。影响雄激素受体(AR)表达的因素尚未得到充分研究。由于MLH1基因甲基化导致的错配修复(MMR)缺陷是子宫内膜癌中最常见的分子改变之一,发生在15%至20%的病例中。MLH1甲基化可能与其他基因的表达降低有关,因此我们研究了MMR状态对AR表达的影响。由于已知NF-κB可诱导AR,因此也对该转录因子进行了研究。对344例未经选择的子宫内膜癌进行了DNA错配修复评估。MLH1甲基化导致MLH1表达缺失被定义为MMR缺陷,MMR蛋白阳性表达被定义为MMR完整。从这组病例中选取了一个由96例2级子宫内膜样腺癌组成的病例对照队列进行研究(47例MMR缺陷,49例MMR完整)。病例在组织类型、分级和年龄方面进行了匹配。AR和NF-κB免疫组化表达通过用于雌激素受体的2种不同评分系统(CAP/ASCO和Allred)进行评估。尽管NF-κB水平较高,但MMR缺陷与AR表达的平均百分比显著降低有关。MMR缺陷组的AR表达更具变异性,在较低范围内评分的病例更多。这些发现对妇科癌症中AR拮抗剂的临床试验具有启示意义。