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上皮-间质转化与癌症干细胞表型:来自癌症生物学的见解及其对结直肠癌的治疗意义

Epithelial-to-mesenchymal transition and the cancer stem cell phenotype: insights from cancer biology with therapeutic implications for colorectal cancer.

作者信息

Findlay V J, Wang C, Watson D K, Camp E R

机构信息

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA.

Division of Surgical Oncology, Department of Surgery, Medical University of South Carolina, Charleston, SC, USA.

出版信息

Cancer Gene Ther. 2014 May;21(5):181-7. doi: 10.1038/cgt.2014.15. Epub 2014 May 2.

DOI:10.1038/cgt.2014.15
PMID:24787239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4041800/
Abstract

Although mortality from colorectal cancer (CRC) is decreasing, CRC is still the second highest cause of cancer-related deaths in America. Chemotherapy and radiation therapy now have central roles in our strategies to fight cancer, although we continue to lack novel strategies overcoming therapeutic resistance. Molecular mechanisms of therapeutic resistance in CRC continue to be under intense investigation. In this review, we highlight the recent evidence linking epithelial-to-mesenchymal transition (EMT) with aggressive tumor biology as well as with the cancer stem cells (CSCs) across multiple organ systems including colon cancer. Furthermore, in the era of neo-adjuvant treatment, the clinical implications are concerning that our treatments may have the potential to induce more aggressive cancer cells through EMT, perhaps even generating CSCs more capable of metastasis and further resistant to treatment. This concern and potential reality highlights the critical need for further understanding the impact of clinical therapy on the pathobiology of cancer and further supports the need to therapeutically target the CSC. Besides serving as potential biomarkers for aggressive tumor biology and therapeutic resistance, EMT and CSC molecular pathways may highlight novel therapeutic targets as strategies for improving the response to conventional anti-neoplastic agents translating into improved oncologic outcomes.

摘要

尽管结直肠癌(CRC)的死亡率正在下降,但CRC仍是美国癌症相关死亡的第二大原因。化疗和放射治疗目前在我们的抗癌策略中发挥着核心作用,尽管我们仍然缺乏克服治疗耐药性的新策略。CRC治疗耐药的分子机制仍在深入研究中。在这篇综述中,我们强调了最近的证据,这些证据将上皮-间质转化(EMT)与侵袭性肿瘤生物学以及包括结肠癌在内的多个器官系统中的癌症干细胞(CSCs)联系起来。此外,在新辅助治疗时代,临床意义在于我们的治疗可能有潜力通过EMT诱导出更具侵袭性的癌细胞,甚至可能产生更具转移能力且对治疗更具抗性的CSCs。这种担忧和潜在现实凸显了进一步了解临床治疗对癌症病理生物学影响的迫切需求,并进一步支持了针对CSC进行治疗的必要性。除了作为侵袭性肿瘤生物学和治疗耐药性的潜在生物标志物外,EMT和CSC分子途径可能会突出新的治疗靶点,作为改善对传统抗肿瘤药物反应的策略,从而转化为更好的肿瘤学结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1d3/4041800/f6fa81b8e813/nihms579969f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1d3/4041800/cc9ac3d9058f/nihms579969f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1d3/4041800/ddc55dc1fba5/nihms579969f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1d3/4041800/f6fa81b8e813/nihms579969f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1d3/4041800/cc9ac3d9058f/nihms579969f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1d3/4041800/ddc55dc1fba5/nihms579969f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1d3/4041800/f6fa81b8e813/nihms579969f3.jpg

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