Department of Breast Cancer, Guangdong Provincial People's Hospital and Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, China; School of Medicine, South China University of Technology, 106 Zhongshan Er Road, Guangzhou 510080, Guangdong, China.
Department of Breast Cancer, Guangdong Provincial People's Hospital and Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, China; School of Medicine, South China University of Technology, 106 Zhongshan Er Road, Guangzhou 510080, Guangdong, China;; The Second School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong, China;; Shantou University Medical College, Shantou, Guangdong, China.
EBioMedicine. 2021 Sep;71:103542. doi: 10.1016/j.ebiom.2021.103542. Epub 2021 Aug 26.
Patients with breast cancer presenting with single lymph node metastasis (from a sentinel node) experience prolonged survival compared to patients with multiple lymph node metastases (≥3). However, little information is available on the genetic and immunological characteristics of breast cancer metastases within the regional lymph nodes as they progress from the sentinel lymph node (SLN) downstream to multiple regional lymph nodes (MLNs).
Genomic profiling was performed using a next-generation sequencing panel covering 520 cancer-related genes in the primary tumour and metastatic lymph nodes of 157 female patients with breast cancer. We included primary tumours, metastatic lymph nodes and adjacent clinically normal lymph nodes (20 patients from the SLN group and 28 patients from the MLNs group) in the whole transcriptome analysis.
The downstream metastatic lymph nodes (P = 0.029) and the primary breast tumours (P = 0.011) had a higher frequency of PIK3CA mutations compared to the SLN metastasis. We identified a distinct group of 14 mutations from single sentinel node metastasis and a different group of 15 mutations from multiple nodal metastases. Only 4 distinct mutations (PIK3CA, CDK4, NFKBIA and CDKN1B) were conserved in metastases from both lymph node settings. The tumour mutational burden (TMB) was significantly lower in single nodal metastasis compared to the paired primary breast cancer (P = 0.0021), while the decline in TMB did not reach statistical significance in the MLNs group (P = 0.083). In the gene set enrichment analysis, we identified 4 upregulated signatures in both primary tumour and nodal metastases from the MLNs group, including 3 Epithelial-mesenchymal transition(EMT) signatures and 1 angiogenesis signature. Both the CD8/Treg ratio and the CD8/EMT ratio were significantly higher in adjacent normal lymph nodes from patients with a single metastasis in the SLN compared with samples from the MLNs group (P = 0.045 and P = 0.023, respectively). This suggests that the immune defence from the MLNs patients might have a less favourable microenvironment, thus permitting multiple lymph nodes metastasis.
Single lymph node metastases and multiple lymph node metastases have significant differences in their molecular profiles and immune profiles. The findings are associated with more aggressive tumour characteristics and less favourable immune charactoristics in patients with multiple nodal metastases compared to those with a single metastasis in the sentinel node.
This work was supported by funds from High-level Hospital Construction Project (DFJH201921), the National Natural Science Foundation of China (81902828 and 82002928), the Fundamental Research Funds for the Central Universities (y2syD2192230), and the Medical Scientific Research Foundation of Guangdong Province (B2019039).
与存在多个淋巴结转移(≥3 个)的患者相比,仅存在单个淋巴结转移(前哨淋巴结)的乳腺癌患者的生存时间更长。然而,关于从前哨淋巴结(SLN)下游转移至多个区域淋巴结(MLN)时,区域淋巴结内乳腺癌转移的遗传和免疫特征的信息很少。
对 157 例女性乳腺癌患者的原发肿瘤和转移性淋巴结进行了下一代测序面板的基因组分析,该面板涵盖了 520 个与癌症相关的基因。我们对原发性肿瘤、转移性淋巴结和临床相邻正常淋巴结(20 例 SLN 组和 28 例 MLN 组)进行了全转录组分析。
下游转移性淋巴结(P=0.029)和原发性乳腺癌(P=0.011)与 SLN 转移相比,PIK3CA 突变的频率更高。我们从单个 SLN 转移中鉴定出一组 14 个突变,从多个淋巴结转移中鉴定出一组 15 个突变。只有 4 个独特的突变(PIK3CA、CDK4、NFKBIA 和 CDKN1B)在两种淋巴结转移中均存在。与配对的原发性乳腺癌相比,单个淋巴结转移的肿瘤突变负担(TMB)显著降低(P=0.0021),而在 MLN 组中 TMB 的下降没有达到统计学意义(P=0.083)。在基因集富集分析中,我们在来自 MLN 组的原发性肿瘤和淋巴结转移中均鉴定出 4 个上调的特征,包括 3 个上皮-间充质转化(EMT)特征和 1 个血管生成特征。与 MLN 组相比,在 SLN 中单个转移的患者的相邻正常淋巴结中,CD8/Treg 比值和 CD8/EMT 比值均显著升高(P=0.045 和 P=0.023)。这表明 MLN 患者的免疫防御可能具有不太有利的微环境,从而允许多个淋巴结转移。
单个淋巴结转移和多个淋巴结转移在分子谱和免疫谱方面存在显著差异。与 SLN 中存在单个转移的患者相比,多个淋巴结转移患者的发现与更具侵袭性的肿瘤特征和较差的免疫特征相关。
本工作得到高水平医院建设项目(DFJH201921)、国家自然科学基金(81902828 和 82002928)、中央高校基本科研业务费(y2syD2192230)和广东省医学科研基金(B2019039)的支持。