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Revisiting 'Hallmarks of Cancer' In Sarcomas.

作者信息

Honoki Kanya, Tsujiuchi Toshifumi, Kishi Shingo, Kuniyasu Hiroki

机构信息

Dept. Of Orthopedic Oncology & Reconstructive Medicine, Nara Medical University, Japan.

Dept. of Life Sciences, Kindai University, Japan.

出版信息

J Cancer. 2024 Feb 4;15(7):1786-1804. doi: 10.7150/jca.92844. eCollection 2024.


DOI:10.7150/jca.92844
PMID:38434982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10905407/
Abstract

There is no doubt that anyone who has participated in cancer care or research has once read the 'Hallmarks of Cancer' papers published by Hanahan and Weinberg in 2001 and 2011. They initially defined the six qualities of cancer cells as cancer hallmarks in 2001, but expanded that to 11 as a next generation in 2011. In their papers, they discussed the potential treatment strategies against cancer corresponding to each of the 11 hallmarks, and to date, proposed therapies that target genes and signaling pathways associated with each of these hallmarks have guided a trail that cancer treatments should take, some of which are now used as standard in clinical practice and some of which have yet to progress that far. Along with the recent advances in cancer research such as genomic analysis with next generation sequencing, they can be reconverged to an alternative six categories defined as selective proliferative advantages, altered stress response, deregulated cellular metabolism, immune modulation and inflammation, tumor microenvironment, tissue invasion and metastasis. In this paper, we will overview the current state of these alternative hallmarks and their corresponding treatments in the current sarcoma practice, then discuss the future direction of sarcoma treatment.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/9830334b28bf/jcav15p1786g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/1b0c8c24e2c1/jcav15p1786g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/50c6e50015d6/jcav15p1786g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/9940a9ba2985/jcav15p1786g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/13d0a2af5c70/jcav15p1786g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/e60beb678c26/jcav15p1786g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/c2abe4068956/jcav15p1786g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/e4b9842a8d1a/jcav15p1786g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/6dd09d585de6/jcav15p1786g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/9830334b28bf/jcav15p1786g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/1b0c8c24e2c1/jcav15p1786g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/50c6e50015d6/jcav15p1786g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/9940a9ba2985/jcav15p1786g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/13d0a2af5c70/jcav15p1786g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/e60beb678c26/jcav15p1786g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/c2abe4068956/jcav15p1786g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/e4b9842a8d1a/jcav15p1786g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/6dd09d585de6/jcav15p1786g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b6/10905407/9830334b28bf/jcav15p1786g009.jpg

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[5]
Clinical sequencing of soft tissue and bone sarcomas delineates diverse genomic landscapes and potential therapeutic targets.

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[6]
Clinical genomic profiling in the management of patients with soft tissue and bone sarcoma.

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[7]
Cancer treatments should benefit patients: a common-sense revolution in oncology.

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[8]
Clinical Utility of Genomic Profiling in the Treatment of Advanced Sarcomas: A Single-Center Experience.

JCO Precis Oncol. 2018-11

[9]
Resistance to natural killer cell immunosurveillance confers a selective advantage to polyclonal metastasis.

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[10]
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