Department of Surgery, University of California, San Francisco, San Francisco, California, United States of America.
UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California, United States of America.
PLoS One. 2023 Apr 6;18(4):e0271354. doi: 10.1371/journal.pone.0271354. eCollection 2023.
Tumors rich in stroma are associated with advanced stage and poor prognosis in colorectal adenocarcinoma (CRC). Abundance of stromal cells also has implications for genomic analysis of patient tumors as it may prevent detection of somatic mutations. As part of our efforts to interrogate stroma-cancer cell interactions and to identify actionable therapeutic targets in metastatic CRC, we aimed to determine the proportion of stroma embedded in hepatic CRC metastases by performing computational tumor purity analysis based on whole exome sequencing data (WES). Unlike previous studies focusing on histopathologically prescreened samples, we used an unbiased in-house collection of tumor specimens. WES from CRC liver metastasis samples were utilized to evaluate stromal content and to assess the performance of three in silico tumor purity tools, ABSOLUTE, Sequenza and PureCN. Matching tumor derived organoids were analyzed as a high purity control as they are enriched in cancer cells. Computational purity estimates were compared to those from a histopathological assessment conducted by a board-certified pathologist. According to all computational methods, metastatic specimens had a median tumor purity of 30% whereas the organoids were enriched for cancer cells with a median purity estimate of 94%. In line with this, variant allele frequencies (VAFs) of oncogenes and tumor suppressor genes were undetectable or low in most patient tumors, but higher in matching organoid cultures. Positive correlation was observed between VAFs and in silico tumor purity estimates. Sequenza and PureCN produced concordant results whereas ABSOLUTE yielded lower purity estimates for all samples. Our data shows that unbiased sample selection combined with molecular, computational, and histopathological tumor purity assessment is critical to determine the level of stroma embedded in metastatic colorectal adenocarcinoma.
富含基质的肿瘤与结直肠腺癌 (CRC) 的晚期和预后不良相关。基质细胞的丰度也对患者肿瘤的基因组分析有影响,因为它可能会阻止体细胞突变的检测。作为我们努力研究基质-癌细胞相互作用并确定转移性 CRC 中可行的治疗靶点的一部分,我们旨在通过基于全外显子组测序数据 (WES) 进行计算肿瘤纯度分析来确定嵌入肝 CRC 转移瘤中的基质比例。与之前专注于组织病理学预筛选样本的研究不同,我们使用了我们内部收集的肿瘤标本的无偏样本。利用 CRC 肝转移样本的 WES 来评估基质含量,并评估三种计算机肿瘤纯度工具,即 ABSOLUTE、Sequenza 和 PureCN 的性能。匹配的肿瘤衍生类器官被分析为高纯度对照,因为它们富含癌细胞。计算纯度估计值与由认证病理学家进行的组织病理学评估进行比较。根据所有计算方法,转移性标本的中位数肿瘤纯度为 30%,而类器官富含癌症细胞,中位数纯度估计值为 94%。与此一致的是,大多数患者肿瘤中的癌基因和肿瘤抑制基因的变异等位基因频率 (VAF) 无法检测到或较低,但在匹配的类器官培养物中较高。VAF 与计算机肿瘤纯度估计值之间存在正相关。Sequenza 和 PureCN 产生了一致的结果,而 ABSOLUTE 对所有样本的纯度估计值较低。我们的数据表明,无偏样本选择与分子、计算和组织病理学肿瘤纯度评估相结合对于确定转移性结直肠腺癌中嵌入的基质水平至关重要。