Pickup Michael W, Mouw Janna K, Weaver Valerie M
Department of Surgery, Center for Bioengineering and Tissue Regeneration UCSF, San Francisco, CA, USA.
Department of Surgery, Center for Bioengineering and Tissue Regeneration UCSF, San Francisco, CA, USA Departments of Anatomy, Bioengineering and Therapeutic Sciences, UCSF, San Francisco, CA, USA Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research UCSF, San Francisco, CA, USA UCSF Helen Diller Comprehensive Cancer Center UCSF, San Francisco, CA, USA
EMBO Rep. 2014 Dec;15(12):1243-53. doi: 10.15252/embr.201439246. Epub 2014 Nov 8.
The extracellular matrix regulates tissue development and homeostasis, and its dysregulation contributes to neoplastic progression. The extracellular matrix serves not only as the scaffold upon which tissues are organized but provides critical biochemical and biomechanical cues that direct cell growth, survival, migration and differentiation and modulate vascular development and immune function. Thus, while genetic modifications in tumor cells undoubtedly initiate and drive malignancy, cancer progresses within a dynamically evolving extracellular matrix that modulates virtually every behavioral facet of the tumor cells and cancer-associated stromal cells. Hanahan and Weinberg defined the hallmarks of cancer to encompass key biological capabilities that are acquired and essential for the development, growth and dissemination of all human cancers. These capabilities include sustained proliferation, evasion of growth suppression, death resistance, replicative immortality, induced angiogenesis, initiation of invasion, dysregulation of cellular energetics, avoidance of immune destruction and chronic inflammation. Here, we argue that biophysical and biochemical cues from the tumor-associated extracellular matrix influence each of these cancer hallmarks and are therefore critical for malignancy. We suggest that the success of cancer prevention and therapy programs requires an intimate understanding of the reciprocal feedback between the evolving extracellular matrix, the tumor cells and its cancer-associated cellular stroma.
细胞外基质调节组织发育和内环境稳定,其失调会导致肿瘤进展。细胞外基质不仅作为组织构建的支架,还提供关键的生化和生物力学信号,指导细胞生长、存活、迁移和分化,并调节血管发育和免疫功能。因此,虽然肿瘤细胞中的基因改变无疑启动并驱动了恶性肿瘤的发生,但癌症是在一个动态演变的细胞外基质中进展的,该基质几乎调节着肿瘤细胞和癌症相关基质细胞的每一个行为方面。哈纳汉和温伯格将癌症的特征定义为包括所有人类癌症发生、生长和扩散所必需的关键生物学能力。这些能力包括持续增殖、逃避生长抑制、抗死亡、复制永生、诱导血管生成、侵袭起始、细胞能量代谢失调、逃避免疫破坏和慢性炎症。在此,我们认为来自肿瘤相关细胞外基质的生物物理和生化信号影响这些癌症特征中的每一个,因此对恶性肿瘤至关重要。我们认为,癌症预防和治疗方案的成功需要深入了解不断演变的细胞外基质、肿瘤细胞及其癌症相关细胞基质之间的相互反馈。