Cancer Biology, Stem CentRx, Inc., South San Francisco, CA 94080, USA.
Lab Invest. 2013 Sep;93(9):970-82. doi: 10.1038/labinvest.2013.92. Epub 2013 Aug 5.
Cancer is a heterogeneous disease manifest in many forms. Tumor histopathology can differ significantly among patients and cellular heterogeneity within tumors is common. A primary goal of cancer biologists is to better understand tumorigenesis and cancer progression; however, the complex nature of tumors has posed a substantial challenge to unlocking cancer's secrets. The cancer stem cell (CSC) paradigm for the pathobiology of solid tumors appropriately acknowledges phenotypic and functional tumor cell heterogeneity observed in solid tumors and accounts for the disconnect between drug approval based on response and the general inability of approved therapies to meaningfully impact survival due to their failure to eradicate these most important of cellular targets. First proposed to exist decades ago, CSC have only recently begun to be precisely identified due to technical advancements that facilitate identification, isolation, and interrogation of distinct tumor cell subpopulations with differing ability to form and perpetuate tumors. Precise identification of CSC populations and the complete hierarchy of cells within solid tumors will facilitate more accurate characterization of patient subtypes and ultimately contribute to more personalized and effective therapies. Rapid advancement in the understanding of tumor biology as it exists in patients requires cooperation among institutions, surgeons, pathologists, cancer biologists and patients alike, primarily because this translational research is best done with patient-derived tissue grown in the xenograft setting as patient-derived xenografts. This review calls for a broader change in the approaches taken to study cancer pathobiology, highlights what implications the CSC paradigm has for pathologists and cancer biologists alike, and calls for greater collaboration between institutions, physicians and scientists in order to more rapidly advance our collective understanding of cancer.
癌症是一种表现形式多样的异质性疾病。肿瘤组织病理学在患者之间可能存在显著差异,肿瘤内的细胞异质性也很常见。癌症生物学家的主要目标是更好地理解肿瘤发生和癌症进展;然而,肿瘤的复杂性给揭示癌症的秘密带来了巨大挑战。实体瘤的癌症干细胞 (CSC) 发病机制模型恰当地承认了实体瘤中观察到的表型和功能肿瘤细胞异质性,并解释了基于反应批准药物与批准疗法普遍无法显著影响生存之间的脱节,因为它们未能根除这些最重要的细胞靶标。CSC 最初被提出存在于几十年前,直到最近,由于技术的进步,才能够精确识别它们,这些技术有助于识别、分离和研究具有不同形成和维持肿瘤能力的不同肿瘤细胞亚群。精确识别 CSC 群体和实体瘤内的完整细胞层次结构将有助于更准确地描述患者亚型,并最终有助于更个性化和有效的治疗。随着对患者体内肿瘤生物学的理解的快速进展,需要机构、外科医生、病理学家、癌症生物学家和患者之间的合作,主要是因为这种转化研究最好是在患者来源的组织在异种移植环境中生长的情况下进行,即患者来源的异种移植物。这篇综述呼吁在研究癌症发病机制的方法上进行更广泛的改变,强调了 CSC 范式对病理学家和癌症生物学家的影响,并呼吁机构、医生和科学家之间加强合作,以便更迅速地提高我们对癌症的集体认识。