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Characterization of Distinct Populations of Carcinoma-Associated Fibroblasts from Non–Small Cell Lung Carcinoma Reveals a Role for ST8SIA2 in Cancer Cell Invasion

Carcinoma-associated fibroblasts (CAFs) are abundant stromal cells in tumor microenvironment that are critically involved in cancer progression. Contrasting reports have shown that CAFs can have either pro- or antitumorigenic roles, indicating that CAFs are functionally heterogeneous. Therefore, to...

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Published in:Neoplasia (New York, N.Y.) N.Y.), 2019-05, Vol.21 (5), p.482-493
Main Authors: Hao, Jing, Zeltz, Cédric, Pintilie, Melania, Li, Quan, Sakashita, Shingo, Wang, Tao, Cabanero, Michael, Martins-Filho, Sebastiao N., Wang, Dennis Y., Pasko, Elena, Venkat, Kalpana, Joseph, Joella, Raghavan, Vibha, Zhu, Chang-Qi, Wang, Yu-Hui, Moghal, Nadeem, Tsao, Ming-Sound, Navab, Roya
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cited_by cdi_FETCH-LOGICAL-c528t-8fd92a98c39446b6327599c70258273c509082ba266859b98384a97eac5f99f83
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container_title Neoplasia (New York, N.Y.)
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creator Hao, Jing
Zeltz, Cédric
Pintilie, Melania
Li, Quan
Sakashita, Shingo
Wang, Tao
Cabanero, Michael
Martins-Filho, Sebastiao N.
Wang, Dennis Y.
Pasko, Elena
Venkat, Kalpana
Joseph, Joella
Raghavan, Vibha
Zhu, Chang-Qi
Wang, Yu-Hui
Moghal, Nadeem
Tsao, Ming-Sound
Navab, Roya
description Carcinoma-associated fibroblasts (CAFs) are abundant stromal cells in tumor microenvironment that are critically involved in cancer progression. Contrasting reports have shown that CAFs can have either pro- or antitumorigenic roles, indicating that CAFs are functionally heterogeneous. Therefore, to precisely target the cancer-promoting CAF subsets, it is necessary to identify specific markers to define these subpopulations and understand their functions. We characterized two CAFs subsets from 28 non–small cell lung cancer (NSCLC) patient tumors that were scored and classified based on desmoplasia [mainly characterized by proliferating CAFs; high desmoplastic CAFs (HD-CAF; n = 15) and low desmoplastic CAFs (LD-CAF; n = 13)], which is an independent prognostic factor. Here, for the first time, we demonstrate that HD-CAFs and LD-CAFs show different tumor-promoting abilities. HD-CAFs showed higher rate of collagen matrix remodeling, invasion, and tumor growth compared to LD-CAFs. Transcriptomic analysis identified 13 genes that were differentially significant (fold ≥1.5; adjusted P value < .1) between HD-CAFs and LD-CAFs. The top upregulated differentially expressed gene, ST8SIA2 (11.3 fold; adjusted P value = .02), enhanced NSCLC tumor cell invasion in 3D culture compared to control when it was overexpressed in CAFs, suggesting an important role of ST8SIA2 in cancer cell invasion. We confirmed the protumorigenic role of ST8SIA2, showing that ST8SIA2 was significantly associated with the risk of relapse in three independent NSCLC clinical datasets. In summary, our studies show that functional heterogeneity in CAF plays key role in promoting cancer cell invasion in NSCLC.
doi_str_mv 10.1016/j.neo.2019.03.009
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Contrasting reports have shown that CAFs can have either pro- or antitumorigenic roles, indicating that CAFs are functionally heterogeneous. Therefore, to precisely target the cancer-promoting CAF subsets, it is necessary to identify specific markers to define these subpopulations and understand their functions. We characterized two CAFs subsets from 28 non–small cell lung cancer (NSCLC) patient tumors that were scored and classified based on desmoplasia [mainly characterized by proliferating CAFs; high desmoplastic CAFs (HD-CAF; n = 15) and low desmoplastic CAFs (LD-CAF; n = 13)], which is an independent prognostic factor. Here, for the first time, we demonstrate that HD-CAFs and LD-CAFs show different tumor-promoting abilities. HD-CAFs showed higher rate of collagen matrix remodeling, invasion, and tumor growth compared to LD-CAFs. Transcriptomic analysis identified 13 genes that were differentially significant (fold ≥1.5; adjusted P value &lt; .1) between HD-CAFs and LD-CAFs. The top upregulated differentially expressed gene, ST8SIA2 (11.3 fold; adjusted P value = .02), enhanced NSCLC tumor cell invasion in 3D culture compared to control when it was overexpressed in CAFs, suggesting an important role of ST8SIA2 in cancer cell invasion. We confirmed the protumorigenic role of ST8SIA2, showing that ST8SIA2 was significantly associated with the risk of relapse in three independent NSCLC clinical datasets. 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subjects Animals
Biomarkers, Tumor - genetics
Biomarkers, Tumor - metabolism
Cancer-Associated Fibroblasts - metabolism
Cancer-Associated Fibroblasts - pathology
Carcinoma, Non-Small-Cell Lung - genetics
Carcinoma, Non-Small-Cell Lung - metabolism
Carcinoma, Non-Small-Cell Lung - pathology
Cell Movement
Cell Proliferation
Cohort Studies
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Humans
Lung Neoplasms - genetics
Lung Neoplasms - metabolism
Lung Neoplasms - pathology
Male
Mice
Mice, SCID
Neoplasm Invasiveness
Neoplasm Recurrence, Local - genetics
Neoplasm Recurrence, Local - metabolism
Neoplasm Recurrence, Local - pathology
Prognosis
Sialyltransferases - genetics
Sialyltransferases - metabolism
Stromal Cells - metabolism
Stromal Cells - pathology
Survival Rate
Tumor Cells, Cultured
Xenograft Model Antitumor Assays
title Characterization of Distinct Populations of Carcinoma-Associated Fibroblasts from Non–Small Cell Lung Carcinoma Reveals a Role for ST8SIA2 in Cancer Cell Invasion
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