Blocking KRAS Signaling for the Treatment of Lung Cancer: Mission Possible?
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- Horio Yoshitsugu
- Department of Outpatient Services, Aichi Cancer Center Hospital Department of Thoracic Oncology, Aichi Cancer Center Hospital
Bibliographic Information
- Other Title
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- KRAS変異陽性肺がんの薬物療法は開発されるか?
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Description
<p>The three RAS oncogenes with high homology, considered to be undruggable, are the most frequently (approximately 25%) mutated gene family in human cancer. Missense mutations of the KRAS gene occur predominantly at codons 12, 13 or 61 and are observed in 30% of patients with lung adenocarcinoma in North American populations and 10% of those in Japanese populations. Although comprehensive efforts to develop therapeutic strategies to block the mutant RAS function, which is involved in the growth and development of cancer, have been made, clinically effective anti-RAS therapies have remained elusive for more than 30 years since the discovery of the RAS oncogenes in the 1980s. Therefore, in 2013, the National Cancer Institute (NCI) launched an RAS initiative to develop drugs that target the cell signaling pathway controlled by the RAS oncogenes. With research in progress, there is hope that mutant RAS can finally be conquered in the near future. In the present manuscript, I will describe the history of and recent advances in these research efforts.</p>
Journal
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- Haigan
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Haigan 58 (7), 953-958, 2018-12-20
The Japan Lung Cancer Society
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Details 詳細情報について
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- CRID
- 1390845713037984896
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- NII Article ID
- 130007555540
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- ISSN
- 13489992
- 03869628
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- Text Lang
- ja
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed