Divisions of Endocrinology, University of Colorado Anschutz Medical Campus, Mail Stop 8106, 12801 E. 17th Avenue, Aurora, CO 80045, USA.
Horm Cancer. 2013 Jun;4(3):140-53. doi: 10.1007/s12672-013-0136-z. Epub 2013 Mar 12.
Pregnancy-associated breast cancers (PABC) generally present at advanced stages and have a poor prognosis. The reasons are unclear but we hypothesized that the continuous high levels of estrogens and progesterone were involved. We have now carried out a detailed analysis of PABC compared to tumors of age-matched nonpregnant (non-PABC) women. Malignant epithelia and tumor-associated stroma of PABC and non-PABC were isolated by laser capture microdissection and gene expression profiled. Additionally, normal breast epithelia and stroma adjacent to the two tumor types were analyzed. Lastly, subsets of previously identified E- and P-regulated genes were defined in all tissues. We find that PABC signatures cluster with established breast cancer subtypes. Major hormone-regulated genes whose expression correlated with epithelia of PABC dealt with regulation of cell proliferation, metabolism, and tumor aggressiveness, including genes used to predict tumor recurrence. Compared to normal epithelia, a significant number of genes associated with cell cycle processes were enriched in PABC, many of which are hormone regulated. Thus, compared to normal epithelia, many of the genes that were differentially expressed in epithelia of PABC were distinct from those differentially expressed in non-PABC. With regard to the tumor microenvironment, immune-related genes were enriched in tumor-associated stroma of PABC. Compared to normal stroma, PABC-associated stroma overexpressed immune response genes, while genes involved in angiogenesis and extracellular matrix deposition were more commonly downregulated. This suggests that the heightened aggressiveness of PABC may involve a predisposition to metastasis through extracellular matrix degradation, plus angiogenesis independence. Moreover, genes encoding cell proliferative factors, signaling, immunomodulators and cell death, were hormone regulated in stroma. In sum, these analyses demonstrate complex patterns of enrichment and hormonal regulation of genes in PABC and suggest that it may have a distinct biological nature.
妊娠相关性乳腺癌(PABC)通常在晚期出现,预后较差。原因尚不清楚,但我们假设持续高水平的雌激素和孕激素与此有关。我们现在对 PABC 与年龄匹配的非妊娠(非 PABC)妇女的肿瘤进行了详细分析。通过激光捕获显微切割分离 PABC 和非 PABC 的恶性上皮和肿瘤相关基质,并进行基因表达谱分析。此外,还分析了两种肿瘤类型相邻的正常乳腺上皮和基质。最后,在所有组织中定义了先前确定的 E 和 P 调节基因的亚组。我们发现 PABC 特征与已建立的乳腺癌亚型聚类。与 PABC 上皮相关的表达与激素相关的主要基因调节因子涉及细胞增殖、代谢和肿瘤侵袭性的调节,包括用于预测肿瘤复发的基因。与正常上皮相比,在 PABC 上皮中富集了大量与细胞周期过程相关的基因,其中许多基因受激素调节。因此,与正常上皮相比,在 PABC 上皮中差异表达的许多基因与在非 PABC 上皮中差异表达的基因不同。就肿瘤微环境而言,免疫相关基因在 PABC 的肿瘤相关基质中富集。与正常基质相比,PABC 相关基质过度表达免疫反应基因,而参与血管生成和细胞外基质沉积的基因则更为常见下调。这表明 PABC 的侵袭性增强可能涉及通过细胞外基质降解和血管生成独立性促进转移的倾向。此外,编码细胞增殖因子、信号转导、免疫调节剂和细胞死亡的基因在基质中受激素调节。总之,这些分析表明 PABC 中基因的富集和激素调节具有复杂的模式,并表明其可能具有独特的生物学性质。