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靶向肿瘤微环境:胰腺癌治疗的一种潜在方法。

Targeting the cancer-stroma interaction: a potential approach for pancreatic cancer treatment.

机构信息

Department of Hepatobiliary Surgery, The First Affiliated Hospital of Medical College, Xi'an Jiaotong University, Xi'an, Shaanxi, China.

出版信息

Curr Pharm Des. 2012;18(17):2404-15. doi: 10.2174/13816128112092404.

DOI:10.2174/13816128112092404
PMID:22372501
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3414722/
Abstract

Recent studies have demonstrated that the interaction between the cancer and the stroma, play a key role in the development of pancreatic cancer. The desmoplasia, which consists of fibroblasts, pancreatic stellate cells, lymphatic and vascular endothelial cells, immune cells, pathologic increased nerves, and the extracellular matrix (ECM), creates a complex tumor microenvironment that promotes pancreatic cancer development, invasion, metastasis, and resistance to chemotherapy. Thus, the potential approach for targeting the components of this desmoplastic reaction or the pancreatic tumor microenvironment might represent a novel therapeutic approach to advanced pancreatic carcinoma. Novel therapies that target on the pancreatic tumor microenvironment should become one of the more effective treatments for pancreatic cancer.

摘要

最近的研究表明,癌症与基质之间的相互作用在胰腺癌的发展中起着关键作用。由成纤维细胞、胰腺星状细胞、淋巴管和血管内皮细胞、免疫细胞、病理性增加的神经和细胞外基质(ECM)组成的纤维变性,形成了一个促进胰腺癌发展、侵袭、转移和对化疗耐药的复杂肿瘤微环境。因此,针对这种纤维变性反应或胰腺肿瘤微环境成分的潜在治疗方法可能代表了一种治疗晚期胰腺癌的新方法。靶向胰腺肿瘤微环境的新疗法应该成为治疗胰腺癌的更有效方法之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d9a/3414722/b1c60459198e/nihms389632f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d9a/3414722/7ad5a7c0fbf9/nihms389632f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d9a/3414722/abd1fe04ff6d/nihms389632f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d9a/3414722/acdad68fb109/nihms389632f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d9a/3414722/b1c60459198e/nihms389632f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d9a/3414722/7ad5a7c0fbf9/nihms389632f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d9a/3414722/abd1fe04ff6d/nihms389632f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d9a/3414722/acdad68fb109/nihms389632f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d9a/3414722/b1c60459198e/nihms389632f4.jpg

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Pancreatic cancer cells respond to type I collagen by inducing snail expression to promote membrane type 1 matrix metalloproteinase-dependent collagen invasion.胰腺癌细胞通过诱导 snail 表达来响应 I 型胶原,从而促进膜型 1 基质金属蛋白酶依赖性胶原浸润。
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Targeting the Stromal Pro-Tumoral Hyaluronan-CD44 Pathway in Pancreatic Cancer.靶向胰腺癌基质促肿瘤性透明质酸-CD44 通路。
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