Wang Jie, Figueroa Jonine D, Wallstrom Garrick, Barker Kristi, Park Jin G, Demirkan Gokhan, Lissowska Jolanta, Anderson Karen S, Qiu Ji, LaBaer Joshua
Biodesign Institute, Arizona State University, Tempe, Arizona.
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
Cancer Epidemiol Biomarkers Prev. 2015 Sep;24(9):1332-40. doi: 10.1158/1055-9965.EPI-15-0047. Epub 2015 Jun 12.
Basal-like breast cancer (BLBC) is a rare aggressive subtype that is less likely to be detected through mammographic screening. Identification of circulating markers associated with BLBC could have promise in detecting and managing this deadly disease.
Using samples from the Polish Breast Cancer study, a high-quality population-based case-control study of breast cancer, we screened 10,000 antigens on protein arrays using 45 BLBC patients and 45 controls, and identified 748 promising plasma autoantibodies (AAbs) associated with BLBC. ELISA assays of promising markers were performed on a total of 145 BLBC cases and 145 age-matched controls. Sensitivities at 98% specificity were calculated and a BLBC classifier was constructed.
We identified 13 AAbs (CTAG1B, CTAG2, TP53, RNF216, PPHLN1, PIP4K2C, ZBTB16, TAS2R8, WBP2NL, DOK2, PSRC1, MN1, TRIM21) that distinguished BLBC from controls with 33% sensitivity and 98% specificity. We also discovered a strong association of TP53 AAb with its protein expression (P = 0.009) in BLBC patients. In addition, MN1 and TP53 AAbs were associated with worse survival [MN1 AAb marker HR = 2.25, 95% confidence interval (CI), 1.03-4.91; P = 0.04; TP53, HR = 2.02, 95% CI, 1.06-3.85; P = 0.03]. We found limited evidence that AAb levels differed by demographic characteristics.
These AAbs warrant further investigation in clinical studies to determine their value for further understanding the biology of BLBC and possible detection.
Our study identifies 13 AAb markers associated specifically with BLBC and may improve detection or management of this deadly disease.
基底样乳腺癌(BLBC)是一种罕见的侵袭性亚型,通过乳腺钼靶筛查不太可能被发现。鉴定与BLBC相关的循环标志物可能有助于检测和管理这种致命疾病。
利用波兰乳腺癌研究的样本,这是一项基于人群的高质量乳腺癌病例对照研究,我们使用45例BLBC患者和45例对照在蛋白质阵列上筛选了10,000种抗原,并鉴定出748种与BLBC相关的有前景的血浆自身抗体(AAb)。对总共145例BLBC病例和145例年龄匹配的对照进行了有前景标志物的ELISA检测。计算了98%特异性下的敏感性,并构建了BLBC分类器。
我们鉴定出13种AAb(CTAG1B、CTAG2、TP53、RNF216、PPHLN1、PIP4K2C、ZBTB16、TAS2R8、WBP2NL、DOK2、PSRC1、MN1、TRIM21),它们区分BLBC与对照的敏感性为33%,特异性为98%。我们还发现BLBC患者中TP53 AAb与其蛋白表达之间存在强关联(P = 0.009)。此外,MN1和TP53 AAb与较差的生存率相关[MN1 AAb标志物HR = 2.25,95%置信区间(CI),1.03 - 4.91;P = 0.04;TP53,HR = 2.02,95% CI,1.06 - 3.85;P = 0.03]。我们发现有限的证据表明AAb水平因人口统计学特征而异。
这些AAb值得在临床研究中进一步研究,以确定它们在进一步了解BLBC生物学特性和可能的检测方面的价值。
我们的研究鉴定出13种与BLBC特异性相关的AAb标志物,可能改善这种致命疾病的检测或管理。