Kanojia Deepika, Garg Manoj, Gupta Samir, Gupta Anju, Suri Anil
Cancer Research Program, Cancer Microarray, Genes and Proteins Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, India.
Cancer Epidemiol Biomarkers Prev. 2009 Feb;18(2):630-9. doi: 10.1158/1055-9965.EPI-08-0629. Epub 2009 Feb 3.
To date, there have been no tumor biomarkers validated and incorporated into oncologic practice for the early diagnosis of breast cancer. Recently, we showed that sperm-associated antigen 9 (SPAG9), a member of cancer testis (CT) antigen family, is associated with ovarian carcinomas. In the present study, we investigated SPAG9 expression and humoral immune response in breast cancer. We further evaluated the diagnostic potential of autoantibodies to SPAG9 protein in various stages, grades, and histotypes of breast cancer. We analyzed the association of SPAG9 immunoreactivity score (IRS) with predicted risk of breast cancer recurrence over 10 years. Our reverse transcription-PCR and immunohistochemical analyses revealed SPAG9 expression in 88% breast cancer specimens independent of tumor stages and grades. Further, the humoral immune response against SPAG9 was detected in 80% breast cancer patients with SPAG9-expressing tumors. The linear regression modeling predicted a direct relationship between presence of lymphovascular invasion and high SPAG9 IRS, whereas the univariate and multivariate logistic regression models predicted a strong association of SPAG9 IRS with tumor grade. Further, our data indicated a significant higher trend of SPAG9 IRS with the predicted high risk of breast cancer recurrence. The present investigation reports for the first time SPAG9 expression and humoral immune response in early stages and low-grade breast cancer. Although our data indicated that autoantibodies against SPAG9 represent a promising approach for the development of biomarker, further large-scale validation studies are required to establish its potential use in early diagnosis and monitoring of breast cancer recurrence.
迄今为止,尚无肿瘤生物标志物被验证并纳入肿瘤学实践用于乳腺癌的早期诊断。最近,我们发现精子相关抗原9(SPAG9),一种癌胚(CT)抗原家族成员,与卵巢癌有关。在本研究中,我们调查了SPAG9在乳腺癌中的表达及体液免疫反应。我们进一步评估了针对SPAG9蛋白的自身抗体在乳腺癌不同分期、分级和组织学类型中的诊断潜力。我们分析了SPAG9免疫反应评分(IRS)与预测的10年乳腺癌复发风险之间的关联。我们的逆转录-聚合酶链反应和免疫组织化学分析显示,88%的乳腺癌标本中有SPAG9表达,且与肿瘤分期和分级无关。此外,在80%有SPAG9表达肿瘤的乳腺癌患者中检测到了针对SPAG9的体液免疫反应。线性回归模型预测淋巴管侵犯的存在与高SPAG9 IRS之间存在直接关系,而单变量和多变量逻辑回归模型预测SPAG9 IRS与肿瘤分级密切相关。此外,我们的数据表明SPAG9 IRS与预测的乳腺癌高复发风险有显著更高的趋势。本研究首次报道了早期和低级别乳腺癌中SPAG9的表达及体液免疫反应。尽管我们的数据表明针对SPAG9的自身抗体是开发生物标志物的一种有前景的方法,但仍需要进一步的大规模验证研究来确定其在乳腺癌早期诊断和复发监测中的潜在用途。