• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肺泡祖细胞与肺癌的起源。

Alveolar progenitor cells and the origin of lung cancer.

机构信息

From the, Stem Cell Program and Divisions of Hematology/Oncology and Pulmonary & Respiratory Diseases, Boston Children's Hospital, Boston, MA, USA.

Harvard Stem Cell Institute, Cambridge, MA, USA.

出版信息

J Intern Med. 2021 May;289(5):629-635. doi: 10.1111/joim.13201. Epub 2020 Dec 19.

DOI:10.1111/joim.13201
PMID:33340175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8604037/
Abstract

Lung Cancer is the leading cause of cancer-related deaths worldwide. This is mainly due to late diagnosis and therefore advanced stage of the disease. Understanding the cell of origin of cancer and the processes that lead to its transformation will allow for earlier diagnosis and more accurate prediction of tumour type, ultimately leading to better treatments and lower patient morbidity. In this review, we focus on alveolar type 2 (AT2) cells as the cell of origin of lung adenocarcinoma (LUAD), the most common type of lung cancer. We first elaborate on the different oncogenes that are associated with LUAD and other lung cancers. After, we lay out in detail what is known about AT2 biology, to further delve into AT2 cells as cell of origin for adenocarcinoma. Understanding the precursors of LUAD and identifying the molecular changes during its progression will allow for earlier detection and better molecular targeting of the disease in early stages.

摘要

肺癌是全球癌症相关死亡的主要原因。这主要是由于诊断较晚,因此疾病处于晚期。了解癌症的起源细胞以及导致其转化的过程,将能够实现更早的诊断和更准确地预测肿瘤类型,最终导致更好的治疗和降低患者发病率。在这篇综述中,我们重点关注肺泡 II 型 (AT2) 细胞作为肺腺癌 (LUAD) 的起源细胞,LUAD 是最常见的肺癌类型。我们首先详细阐述了与 LUAD 和其他肺癌相关的不同致癌基因。之后,我们详细介绍了已知的 AT2 生物学知识,以进一步深入探讨 AT2 细胞作为腺癌的起源细胞。了解 LUAD 的前体并确定其进展过程中的分子变化,将能够在早期阶段更早地发现疾病并更好地针对其分子靶点进行治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fea/8604037/c5e88f62751f/nihms-1751477-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fea/8604037/c5e88f62751f/nihms-1751477-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fea/8604037/c5e88f62751f/nihms-1751477-f0001.jpg

相似文献

1
Alveolar progenitor cells and the origin of lung cancer.肺泡祖细胞与肺癌的起源。
J Intern Med. 2021 May;289(5):629-635. doi: 10.1111/joim.13201. Epub 2020 Dec 19.
2
Alveolar type I cells can give rise to KRAS-induced lung adenocarcinoma.肺泡 I 型细胞能够产生 KRAS 诱导的肺腺癌。
Cell Rep. 2023 Dec 26;42(12):113286. doi: 10.1016/j.celrep.2023.113286. Epub 2023 Nov 22.
3
Early-stage lung cancer is driven by a transitional cell state dependent on a KRAS-ITGA3-SRC axis.早期肺癌由依赖于 KRAS-ITGA3-SRC 轴的过渡细胞状态驱动。
EMBO J. 2024 Jul;43(14):2843-2861. doi: 10.1038/s44318-024-00113-5. Epub 2024 May 16.
4
KRAS(G12D) drives lepidic adenocarcinoma through stem-cell reprogramming.KRAS(G12D) 通过干细胞重编程驱动贴壁型腺癌。
Nature. 2023 Jul;619(7971):860-867. doi: 10.1038/s41586-023-06324-w. Epub 2023 Jul 19.
5
An atlas of epithelial cell states and plasticity in lung adenocarcinoma.肺腺癌上皮细胞状态和可塑性图谱。
Nature. 2024 Mar;627(8004):656-663. doi: 10.1038/s41586-024-07113-9. Epub 2024 Feb 28.
6
Alveolar Differentiation Drives Resistance to KRAS Inhibition in Lung Adenocarcinoma.肺泡分化驱动肺腺癌对 KRAS 抑制的耐药性。
Cancer Discov. 2024 Feb 8;14(2):308-325. doi: 10.1158/2159-8290.CD-23-0289.
7
Matrix metalloproteinase-10 promotes Kras-mediated bronchio-alveolar stem cell expansion and lung cancer formation.基质金属蛋白酶-10 促进 Kras 介导的支气管肺泡干细胞扩增和肺癌形成。
PLoS One. 2011;6(10):e26439. doi: 10.1371/journal.pone.0026439. Epub 2011 Oct 17.
8
Modeling diverse genetic subtypes of lung adenocarcinoma with a next-generation alveolar type 2 organoid platform.利用下一代肺泡 II 型类器官平台对肺腺癌的多种遗传亚型进行建模。
Genes Dev. 2022 Aug 1;36(15-16):936-949. doi: 10.1101/gad.349659.122. Epub 2022 Sep 29.
9
Smoking-induced CCNA2 expression promotes lung adenocarcinoma tumorigenesis by boosting AT2/AT2-like cell differentiation.吸烟诱导的 CCNA2 表达通过促进 AT2/AT2 样细胞分化促进肺腺癌肿瘤发生。
Cancer Lett. 2024 Jun 28;592:216922. doi: 10.1016/j.canlet.2024.216922. Epub 2024 May 3.
10
Tumor progression and chromatin landscape of lung cancer are regulated by the lineage factor GATA6.肺癌的肿瘤进展和染色质景观受谱系因子 GATA6 调控。
Oncogene. 2020 Apr;39(18):3726-3737. doi: 10.1038/s41388-020-1246-z. Epub 2020 Mar 10.

引用本文的文献

1
Persistent lineage plasticity driving lung cancer development and progression.持续的谱系可塑性驱动肺癌的发生和发展。
Clin Transl Med. 2025 Aug;15(8):e70458. doi: 10.1002/ctm2.70458.
2
Defining Non-small Cell Lung Cancer Tumor Microenvironment Changes at Primary and Acquired Immune Checkpoint Inhibitor Resistance Using Clinical and Real-World Data.利用临床和真实世界数据定义原发性和获得性免疫检查点抑制剂耐药时非小细胞肺癌肿瘤微环境的变化
Cancer Res Commun. 2025 Jun 1;5(6):1049-1059. doi: 10.1158/2767-9764.CRC-24-0605.
3
Patient-specific gene co-expression networks reveal novel subtypes and predictive biomarkers in lung adenocarcinoma.

本文引用的文献

1
Organoids Model Transcriptional Hallmarks of Oncogenic KRAS Activation in Lung Epithelial Progenitor Cells.类器官模型模拟肺上皮祖细胞中致癌 KRAS 激活的转录特征。
Cell Stem Cell. 2020 Oct 1;27(4):663-678.e8. doi: 10.1016/j.stem.2020.07.022. Epub 2020 Sep 4.
2
Distinct initiating events underpin the immune and metabolic heterogeneity of KRAS-mutant lung adenocarcinoma.KRAS 突变型肺腺癌的免疫和代谢异质性由不同的起始事件驱动。
Nat Commun. 2019 Sep 13;10(1):4190. doi: 10.1038/s41467-019-12164-y.
3
Co-occurring genomic alterations in non-small-cell lung cancer biology and therapy.
患者特异性基因共表达网络揭示了肺腺癌的新亚型和预测性生物标志物。
NPJ Syst Biol Appl. 2025 May 9;11(1):44. doi: 10.1038/s41540-025-00522-0.
4
CD103 T Cells Eliminate Damaged Alveolar Epithelial Type II Cells Under Oxidative Stress to Prevent Lung Tumorigenesis.CD103 T细胞在氧化应激下清除受损的肺泡II型上皮细胞以预防肺癌发生。
Adv Sci (Weinh). 2025 Jul;12(28):e2503557. doi: 10.1002/advs.202503557. Epub 2025 May 8.
5
Current and future therapies for small cell lung carcinoma.小细胞肺癌的当前及未来治疗方法
J Hematol Oncol. 2025 Apr 1;18(1):37. doi: 10.1186/s13045-025-01690-6.
6
The aryl hydrocarbon receptor controls IFN-γ-induced immune checkpoints PD-L1 and IDO via the JAK/STAT pathway in lung adenocarcinoma.芳烃受体通过JAK/STAT途径调控肺腺癌中IFN-γ诱导的免疫检查点PD-L1和IDO。
J Immunol. 2025 Mar 3. doi: 10.1093/jimmun/vkae023.
7
Translating premalignant biology to accelerate non-small-cell lung cancer interception.转化癌前生物学以加速非小细胞肺癌的早期发现。
Nat Rev Cancer. 2025 May;25(5):379-392. doi: 10.1038/s41568-025-00791-1. Epub 2025 Feb 24.
8
KSR1 Mediates Small Cell Lung Carcinoma Tumor Initiation and Cisplatin Resistance.KSR1介导小细胞肺癌的肿瘤起始和顺铂耐药性。
Mol Cancer Res. 2025 Jun 3;23(6):553-566. doi: 10.1158/1541-7786.MCR-24-0652.
9
Aging directs the differential evolution of KRAS-driven lung adenocarcinoma.衰老引导KRAS驱动的肺腺癌的差异进化。
bioRxiv. 2025 Jan 24:2025.01.20.633951. doi: 10.1101/2025.01.20.633951.
10
Development and characterisation of a novel complex triple cell culture model of the human alveolar epithelial barrier.人肺泡上皮屏障新型复杂三细胞培养模型的建立与表征
In Vitro Model. 2024 Aug 6;3(2-3):125-137. doi: 10.1007/s44164-024-00075-2. eCollection 2024 Jun.
非小细胞肺癌生物学和治疗中的共发生基因组改变。
Nat Rev Cancer. 2019 Sep;19(9):495-509. doi: 10.1038/s41568-019-0179-8. Epub 2019 Aug 12.
4
Club cells form lung adenocarcinomas and maintain the alveoli of adult mice.Club 细胞可形成肺腺癌,并维持成年小鼠的肺泡。
Elife. 2019 May 29;8:e45571. doi: 10.7554/eLife.45571.
5
Bronchioalveolar stem cells are a main source for regeneration of distal lung epithelia .肺细支气管肺泡干细胞是远端肺上皮再生的主要来源。
EMBO J. 2019 Jun 17;38(12). doi: 10.15252/embj.2019102099. Epub 2019 Apr 26.
6
Lung regeneration by multipotent stem cells residing at the bronchioalveolar-duct junction.位于支气管肺泡-导管交界处的多能干细胞实现肺再生。
Nat Genet. 2019 Apr;51(4):728-738. doi: 10.1038/s41588-019-0346-6. Epub 2019 Feb 18.
7
Ciliated Muconodular Papillary Tumors of the Lung.肺纤毛黏液结节乳头状肿瘤。
Arch Pathol Lab Med. 2019 Jan;143(1):135-139. doi: 10.5858/arpa.2017-0275-RS. Epub 2018 Oct 24.
8
Regeneration of the lung alveolus by an evolutionarily conserved epithelial progenitor.肺肺泡通过进化保守的上皮祖细胞再生。
Nature. 2018 Mar 8;555(7695):251-255. doi: 10.1038/nature25786. Epub 2018 Feb 28.
9
Single-cell Wnt signaling niches maintain stemness of alveolar type 2 cells.单细胞 Wnt 信号龛维持肺泡 II 型细胞的干性。
Science. 2018 Mar 9;359(6380):1118-1123. doi: 10.1126/science.aam6603. Epub 2018 Feb 1.
10
"Intersections of lung progenitor cells, lung disease and lung cancer." Carla F. Kim. 2017; 26: 170054.“肺祖细胞、肺部疾病与肺癌的交叉点”。卡拉·F·金。2017年;第26期:170054。
Eur Respir Rev. 2017 Oct 25;26(146). doi: 10.1183/16000617.5054-2017. Print 2017 Dec 31.