Dhanota Ninjit, Bal Amanjit, Singh Gurpreet, Arora Sunil K
Department of Immunopathology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Department of Radiation Oncology, Weill Cornell Medicine, New York, USA.
J Clin Transl Res. 2021 Sep 29;7(5):687-700. eCollection 2021 Oct 26.
To delineate the underlying molecular mechanisms responsible for the intratumoral enrichment of breast cancer stem cells (BCSCs) in aggressive breast tumors, we evaluated the frequency and characteristics of BCSCs within the tumor tissue in primary human breast carcinomas. We assessed the expression profiles of various genes in cancer cells (CC) and stromal cells (SC) from these tumors to delineate the role played by the cellular niche in de novo origin or expansion of intra-tumoral cancer stem cells (CSC).
The study included primary tumor and adjacent normal breast tissue specimens from chemotherapy-naïve breast carcinoma patients. The BCSCs, identified as LinCD44CD24 and aldehyde dehydrogenase 1 A1 positive, were enumerated. The flow-cytometrically sorted stromal, and CC were processed for gene expression profiling using a custom-designed polymerase chain reaction array of genes known to facilitate disease progression.
The frequency of BCSCs within the tumor mass correlated significantly with histopathological and molecular grades of tumors, indicating a direct relationship of BCSC with the aggressive behavior of breast cancer. Further, a significantly increased expression of the genes associated with growth factors, cytokines and matricellular proteins in tumors were found in high BCSCs compared to Lo-BCSC tumors, suggesting the possible contribution of stromal and CC in an intratumoral expansion of CSCs. Similarly, a significant upregulation of genes associated with hypoxia and angiogenesis in Hi-BCSCs tumors further supported the role of a hypoxic environment.
Overall, the findings suggest the molecular crosstalk between SC and CC potentially (directly or indirectly) contributes to the expansion of CSC.
The current study highlights the importance of CSC as a potential future predictive/prognostic marker for aggressive breast cancer. The present study predicts the potential risk stratification based on the frequency of BCSCs in primary breast tumors and existing prognostic factors.
为了阐明侵袭性乳腺肿瘤中乳腺癌干细胞(BCSCs)瘤内富集的潜在分子机制,我们评估了原发性人类乳腺癌肿瘤组织内BCSCs的频率和特征。我们评估了这些肿瘤中癌细胞(CC)和基质细胞(SC)中各种基因的表达谱,以阐明细胞微环境在肿瘤内癌干细胞(CSC)的新生起源或扩增中所起的作用。
该研究纳入了未经化疗的乳腺癌患者的原发性肿瘤及相邻正常乳腺组织标本。对鉴定为LinCD44CD24和醛脱氢酶1 A1阳性的BCSCs进行计数。对通过流式细胞术分选的基质细胞和CC进行处理,使用定制设计的已知可促进疾病进展的基因聚合酶链反应阵列进行基因表达谱分析。
肿瘤块内BCSCs的频率与肿瘤的组织病理学和分子分级显著相关,表明BCSC与乳腺癌的侵袭性行为直接相关。此外,与低BCSC肿瘤相比,高BCSC肿瘤中与生长因子、细胞因子和基质细胞蛋白相关的基因表达显著增加,提示基质细胞和CC可能在肿瘤内CSC的扩增中发挥作用。同样,高BCSC肿瘤中与缺氧和血管生成相关的基因显著上调,进一步支持了缺氧环境的作用。
总体而言,研究结果表明SC和CC之间的分子相互作用可能(直接或间接)促进了CSC的扩增。
当前研究强调了CSC作为侵袭性乳腺癌潜在未来预测/预后标志物的重要性。本研究基于原发性乳腺肿瘤中BCSCs的频率和现有预后因素预测了潜在的风险分层。