Transcriptome Analysis of Individual Stromal Cell Populations Identifies Stroma-Tumor Crosstalk in Mouse Lung Cancer Model

Research output: Contribution to journalArticle

Hyejin Choi, Jianting Sheng, Dingcheng Gao, Fuhai Li, Anna Durrans, Seongho Ryu, Sharrell B. Lee, Navneet Narula, Shahin Rafii, Olivier Elemento, NasserK Altorki, Stephen T. Wong, Vivek Mittal

Emerging studies have begun to demonstrate that reprogrammed stromal cells play pivotal roles in tumor growth, metastasis, and resistance to therapy. However, the contribution of stromal cells to non-small-cell lung cancer (NSCLC) has remained underexplored. We used an orthotopic model of Kras-driven NSCLC to systematically dissect the contribution of specific hematopoietic stromal cells in lung cancer. RNA deep-sequencing analysis of individually sorted myeloid lineage and tumor epithelial cells revealed cell-type-specific differentially regulated genes, indicative of activated stroma. We developed a computational model for crosstalk signaling discovery based on ligand-receptor interactions and downstream signaling networks and identified known and novel tumor-stroma paracrine and tumor autocrine crosstalk-signaling pathways in NSCLC. We provide cellular and molecular insights into components of the lung cancer microenvironment that contribute tocarcinogenesis. This study has the potential for development of therapeutic strategies that target tumor-stroma interactions and may complement conventional anti-cancer treatments.

Original languageEnglish (US)
Pages (from-to)1187-1201
Number of pages15
JournalCell Reports
Volume10
Issue number7
DOIs
StatePublished - Feb 24 2015

PMID: 25704820

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Transcriptome Analysis of Individual Stromal Cell Populations Identifies Stroma-Tumor Crosstalk in Mouse Lung Cancer Model. / Choi, Hyejin; Sheng, Jianting; Gao, Dingcheng; Li, Fuhai; Durrans, Anna; Ryu, Seongho; Lee, Sharrell B.; Narula, Navneet; Rafii, Shahin; Elemento, Olivier; Altorki, NasserK; Wong, Stephen T.; Mittal, Vivek.

In: Cell Reports, Vol. 10, No. 7, 24.02.2015, p. 1187-1201.

Research output: Contribution to journalArticle

Harvard

Choi, H, Sheng, J, Gao, D, Li, F, Durrans, A, Ryu, S, Lee, SB, Narula, N, Rafii, S, Elemento, O, Altorki, N, Wong, ST & Mittal, V 2015, 'Transcriptome Analysis of Individual Stromal Cell Populations Identifies Stroma-Tumor Crosstalk in Mouse Lung Cancer Model' Cell Reports, vol. 10, no. 7, pp. 1187-1201. https://doi.org/10.1016/j.celrep.2015.01.040

APA

Choi, H., Sheng, J., Gao, D., Li, F., Durrans, A., Ryu, S., ... Mittal, V. (2015). Transcriptome Analysis of Individual Stromal Cell Populations Identifies Stroma-Tumor Crosstalk in Mouse Lung Cancer Model. Cell Reports, 10(7), 1187-1201. https://doi.org/10.1016/j.celrep.2015.01.040

Vancouver

Choi H, Sheng J, Gao D, Li F, Durrans A, Ryu S et al. Transcriptome Analysis of Individual Stromal Cell Populations Identifies Stroma-Tumor Crosstalk in Mouse Lung Cancer Model. Cell Reports. 2015 Feb 24;10(7):1187-1201. https://doi.org/10.1016/j.celrep.2015.01.040

Author

Choi, Hyejin ; Sheng, Jianting ; Gao, Dingcheng ; Li, Fuhai ; Durrans, Anna ; Ryu, Seongho ; Lee, Sharrell B. ; Narula, Navneet ; Rafii, Shahin ; Elemento, Olivier ; Altorki, NasserK ; Wong, Stephen T. ; Mittal, Vivek. / Transcriptome Analysis of Individual Stromal Cell Populations Identifies Stroma-Tumor Crosstalk in Mouse Lung Cancer Model. In: Cell Reports. 2015 ; Vol. 10, No. 7. pp. 1187-1201.

BibTeX

@article{38a1aab9f1214767a81dad0a128820b3,
title = "Transcriptome Analysis of Individual Stromal Cell Populations Identifies Stroma-Tumor Crosstalk in Mouse Lung Cancer Model",
abstract = "Emerging studies have begun to demonstrate that reprogrammed stromal cells play pivotal roles in tumor growth, metastasis, and resistance to therapy. However, the contribution of stromal cells to non-small-cell lung cancer (NSCLC) has remained underexplored. We used an orthotopic model of Kras-driven NSCLC to systematically dissect the contribution of specific hematopoietic stromal cells in lung cancer. RNA deep-sequencing analysis of individually sorted myeloid lineage and tumor epithelial cells revealed cell-type-specific differentially regulated genes, indicative of activated stroma. We developed a computational model for crosstalk signaling discovery based on ligand-receptor interactions and downstream signaling networks and identified known and novel tumor-stroma paracrine and tumor autocrine crosstalk-signaling pathways in NSCLC. We provide cellular and molecular insights into components of the lung cancer microenvironment that contribute tocarcinogenesis. This study has the potential for development of therapeutic strategies that target tumor-stroma interactions and may complement conventional anti-cancer treatments.",
author = "Hyejin Choi and Jianting Sheng and Dingcheng Gao and Fuhai Li and Anna Durrans and Seongho Ryu and Lee, {Sharrell B.} and Navneet Narula and Shahin Rafii and Olivier Elemento and NasserK Altorki and Wong, {Stephen T.} and Vivek Mittal",
year = "2015",
month = "2",
day = "24",
doi = "10.1016/j.celrep.2015.01.040",
language = "English (US)",
volume = "10",
pages = "1187--1201",
journal = "Cell Reports",
issn = "2211-1247",
publisher = "Cell Press",
number = "7",

}

RIS

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AU - Choi, Hyejin

AU - Sheng, Jianting

AU - Gao, Dingcheng

AU - Li, Fuhai

AU - Durrans, Anna

AU - Ryu, Seongho

AU - Lee, Sharrell B.

AU - Narula, Navneet

AU - Rafii, Shahin

AU - Elemento, Olivier

AU - Altorki, NasserK

AU - Wong, Stephen T.

AU - Mittal, Vivek

PY - 2015/2/24

Y1 - 2015/2/24

N2 - Emerging studies have begun to demonstrate that reprogrammed stromal cells play pivotal roles in tumor growth, metastasis, and resistance to therapy. However, the contribution of stromal cells to non-small-cell lung cancer (NSCLC) has remained underexplored. We used an orthotopic model of Kras-driven NSCLC to systematically dissect the contribution of specific hematopoietic stromal cells in lung cancer. RNA deep-sequencing analysis of individually sorted myeloid lineage and tumor epithelial cells revealed cell-type-specific differentially regulated genes, indicative of activated stroma. We developed a computational model for crosstalk signaling discovery based on ligand-receptor interactions and downstream signaling networks and identified known and novel tumor-stroma paracrine and tumor autocrine crosstalk-signaling pathways in NSCLC. We provide cellular and molecular insights into components of the lung cancer microenvironment that contribute tocarcinogenesis. This study has the potential for development of therapeutic strategies that target tumor-stroma interactions and may complement conventional anti-cancer treatments.

AB - Emerging studies have begun to demonstrate that reprogrammed stromal cells play pivotal roles in tumor growth, metastasis, and resistance to therapy. However, the contribution of stromal cells to non-small-cell lung cancer (NSCLC) has remained underexplored. We used an orthotopic model of Kras-driven NSCLC to systematically dissect the contribution of specific hematopoietic stromal cells in lung cancer. RNA deep-sequencing analysis of individually sorted myeloid lineage and tumor epithelial cells revealed cell-type-specific differentially regulated genes, indicative of activated stroma. We developed a computational model for crosstalk signaling discovery based on ligand-receptor interactions and downstream signaling networks and identified known and novel tumor-stroma paracrine and tumor autocrine crosstalk-signaling pathways in NSCLC. We provide cellular and molecular insights into components of the lung cancer microenvironment that contribute tocarcinogenesis. This study has the potential for development of therapeutic strategies that target tumor-stroma interactions and may complement conventional anti-cancer treatments.

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DO - 10.1016/j.celrep.2015.01.040

M3 - Article

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JO - Cell Reports

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