Department of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Key Laboratory of Breast Cancer in Shanghai, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Cancer Biol Med. 2024 Apr 9;21(5):400-15. doi: 10.20892/j.issn.2095-3941.2023.0492.
Mammographic calcifications are a common feature of breast cancer, but their molecular characteristics and treatment implications in hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) breast cancer remain unclear.
We retrospectively collected mammography records of an HR+/HER2- breast cancer cohort ( = 316) with matched clinicopathological, genomic, transcriptomic, and metabolomic data. On the basis of mammographic images, we grouped tumors by calcification status into calcification-negative tumors, tumors with probably benign calcifications, tumors with calcification of low-moderate suspicion for maligancy and tumors with calcification of high suspicion for maligancy. We then explored the molecular characteristics associated with each calcification status across multiple dimensions.
Among the different statuses, tumors with probably benign calcifications exhibited elevated hormone receptor immunohistochemical staining scores, estrogen receptor (ER) pathway activation, lipid metabolism, and sensitivity to endocrine therapy. Tumors with calcifications of high suspicion for malignancy had relatively larger tumor sizes, elevated lymph node metastasis incidence, Ki-67 staining scores, genomic instability, cell cycle pathway activation, and may benefit from cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors.
Our research established links between tumor calcifications and molecular features, thus proposing potential precision treatment strategies for HR+/HER2- breast cancer.
乳腺钙化是乳腺癌的一个常见特征,但在激素受体阳性(HR+)/人表皮生长因子受体 2 阴性(HER2-)乳腺癌中,其分子特征和治疗意义仍不清楚。
我们回顾性地收集了具有匹配临床病理、基因组、转录组和代谢组学数据的 HR+/HER2-乳腺癌队列(=316)的乳腺 X 线摄影记录。基于乳腺 X 线图像,我们根据钙化状态将肿瘤分为钙化阴性肿瘤、可能良性钙化肿瘤、低中度恶性钙化肿瘤和高度恶性钙化肿瘤。然后,我们从多个维度探索与每种钙化状态相关的分子特征。
在不同的状态中,具有可能良性钙化的肿瘤表现出较高的激素受体免疫组织化学染色评分、雌激素受体(ER)通路激活、脂质代谢和对内分泌治疗的敏感性。具有高度恶性钙化的肿瘤具有相对较大的肿瘤大小、较高的淋巴结转移发生率、Ki-67 染色评分、基因组不稳定性、细胞周期通路激活,可能受益于细胞周期蛋白依赖性激酶 4 和 6(CDK4/6)抑制剂。
我们的研究建立了肿瘤钙化与分子特征之间的联系,从而为 HR+/HER2-乳腺癌提出了潜在的精准治疗策略。