Agarwal Preeti, Khan Fatima, Gupta Sameer, Bhalla Shalini, Thomas Ann, Anand Akshay, Singh Kulranjan, Sonkar Abhinav Arun
Department of Pathology, King George's Medical University, Lucknow, Uttar Pradesh, India.
Department of Surgical Oncology, King George's Medical University, Lucknow, Uttar Pradesh, India.
Clin Pathol. 2022 Feb 14;15:2632010X221076379. doi: 10.1177/2632010X221076379. eCollection 2022 Jan-Dec.
Invasive Breast carcinoma-No special type (NST) is the most common breast malignancy accounting for 95% of breast cancers. Study of predictive and prognostic immunohistochemical markers estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (Her2neu) expression are crucial for treatment planning.
In the present study we studied the hormonal profile in 303 sporadic breast cancers and BRCA1 protein expression in these patients along with its clinico-pathological correlation.
In our patient population, Triple negative Breast carcinoma (TNBC) (104/303; 34.3%) was the most common luminal subtype followed by Luminal A 74/303; 24.4%), Her2 enriched (65/303; 21.5%), and Luminal B (60/303; 19.8%) respectively. This contrasts with many western studies which commonly report Luminal A being the largest subgroup. BRCA1 protein loss was more prominently seen in TNBC (64/104;61.5%) highlighting the possibility that high grade tumors are more susceptible to some epigenetic modifications leading to higher likelihood of loss of BRCA1 protein.
Hence, we conclude that like hereditary cases of breast carcinoma with BRCA1 mutation; BRCA1 loss is also more likely in sporadic TNBC cases.
浸润性乳腺癌-非特殊类型(NST)是最常见的乳腺恶性肿瘤,占乳腺癌的95%。研究预测和预后免疫组化标志物雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子受体2(Her2neu)的表达对于治疗方案的制定至关重要。
在本研究中,我们研究了303例散发性乳腺癌患者的激素谱以及这些患者中BRCA1蛋白的表达及其临床病理相关性。
在我们的患者群体中,三阴性乳腺癌(TNBC)(104/303;34.3%)是最常见的管腔亚型,其次分别是管腔A型(74/303;24.4%)、Her2富集型(65/303;21.5%)和管腔B型(60/303;19.8%)。这与许多西方研究形成对比,那些研究通常报道管腔A型是最大的亚组。BRCA1蛋白缺失在TNBC中更为显著(64/104;61.5%),这突出了高级别肿瘤更容易受到某些表观遗传修饰影响,导致BRCA1蛋白缺失可能性更高的可能性。
因此,我们得出结论,与BRCA1突变的遗传性乳腺癌病例一样;散发性TNBC病例中BRCA1缺失的可能性也更大。