Seabra Mariana Ataydes Leite, Cândido Eduardo Batista, Vidigal Paula Vieira Teixeira, Lamaita Rivia Mara, Rodrigues Angélica Nogueira, Silva Filho Agnaldo Lopes da
Universidade Federal Minas Gerais, Belo Horizonte, MG, Brazil.
Rev Bras Ginecol Obstet. 2018 Feb;40(2):79-85. doi: 10.1055/s-0037-1618597. Epub 2018 Jan 8.
The current study evaluated the expression of WW domain-containing oxidoreductase (WWOX), its association with clinicopathological features and with p53, Ki-67 (cell proliferation) and CD31 (angiogenesis) expression in patients with invasive cervical squamous cell carcinoma (ICSCC). To the best of our knowledge, no other study has evaluated this association.
Women with IB stage-ICSCC ( = 20) and women with uterine leiomyoma ( = 20) were prospectively evaluated. Patients with ICSCC were submitted to type B-C1 radical hysterectomy and pelvic lymphadenectomy. Patients in the control group underwent vaginal hysterectomy. Tissue samples were stained with hematoxylin and eosin for histological evaluation and protein expression was detected by immunohistochemistry studies.
The WWOX expression was significantly lower in the tumor compared with the expression in the benign cervix ( = 0.019). The WWOX expression was inversely associated with the CD31 expression in the tumor samples ( = 0.018). There was no association between the WWOX expression with the p53 expression ( = 0.464) or the Ki-67 expression ( = 0.360) in the samples of invasive carcinoma of the cervix. There was no association between the WWOX expression and tumor size ( = 0.156), grade of differentiation ( = 0.914), presence of lymphatic vascular invasion ( = 0.155), parametrium involvement ( = 0.421) or pelvic lymph node metastasis ( = 0.310) in ICSCC tissue samples.
The results suggested that WWOX may be involved in ICSCC carcinogenesis, and this marker was associated with tumor angiogenesis.
本研究评估含WW结构域氧化还原酶(WWOX)的表达,及其与浸润性宫颈鳞状细胞癌(ICSCC)患者临床病理特征、p53、Ki-67(细胞增殖)和CD31(血管生成)表达的相关性。据我们所知,尚无其他研究评估过这种相关性。
对20例IB期ICSCC患者和20例子宫平滑肌瘤患者进行前瞻性评估。ICSCC患者接受B-C1型根治性子宫切除术和盆腔淋巴结清扫术。对照组患者接受经阴道子宫切除术。组织样本用苏木精和伊红染色进行组织学评估,并通过免疫组织化学研究检测蛋白表达。
与良性宫颈组织中的表达相比,肿瘤组织中WWOX的表达显著降低(P = 0.019)。肿瘤样本中WWOX的表达与CD31的表达呈负相关(P = 0.018)。在宫颈浸润癌样本中,WWOX的表达与p53的表达(P = 0.464)或Ki-67的表达(P = 0.360)之间无相关性。在ICSCC组织样本中,WWOX的表达与肿瘤大小(P = 0.156)、分化程度(P = 0.914)、淋巴管浸润情况(P = 0.155)、宫旁组织受累情况(P = 0.421)或盆腔淋巴结转移情况(P = 0.310)之间无相关性。
结果表明,WWOX可能参与ICSCC的致癌过程,且该标志物与肿瘤血管生成有关。