Intra-tumoral YAP and TAZ heterogeneity drives collective NSCLC invasion that is targeted by SUMOylation inhibitor TAK-981

Non-small cell lung cancer (NSCLC) collective invasion is supported by cooperativity of proliferative (follower) and invasive (leader) cells. H1299-isolated follower cells exhibit higher Yes-associated protein (YAP) expression, while leader cells were found to express elevated transcriptional coactivator with PDZ-binding motif (TAZ/WWTR1) expression. Suppressing TAZ (not YAP) in leader cells reduced invasion. TAZ-regulated leader cell invasion is associated with activation of the EGFR-PI3K-AKT axis. NSCLC patient samples also demonstrated heterogeneity in YAP and TAZ expression. YAP and TAZ regulate proliferation of follower and leader cells. Our results highlight the need to inhibit both YAP and TAZ to effectively target their regulation of collective invasion. We identify that the SUMOylation inhibitor TAK-981 reduces YAP and TAZ expression, decreasing tumor burden and metastasis in a murine NSCLC model. Our study reveals an intra-tumoral division of labor, driven by differential YAP and TAZ expression, which can be effectively targeted with TAK-981 for NSCLC therapy.

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Publication Details

Journal
iScience
Published
2024-10-11
DOI
https://doi.org/10.1016/j.isci.2024.111133
Citations
6
Primary Topic
Hippo pathway signaling and YAP/TAZ
Type
article
Field-Weighted Citation Impact
1.96

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article

Intra-tumoral YAP and TAZ heterogeneity drives collective NSCLC invasion that is targeted by SUMOylation inhibitor TAK-981

Junghui Koo, Madhusmita Behera, Shi‐Yong Sun, Pratik Shriwas et al.
6 citations
iScience
Hippo pathway signaling and YAP/TAZ
1.96
article

Intra-tumoral YAP and TAZ heterogeneity drives collective NSCLC invasion that is targeted by SUMOylation inhibitor TAK-981

Junghui Koo, Madhusmita Behera, Shi‐Yong Sun, Pratik Shriwas, Janna K. Mouw, Carol Tucker‐Burden, Mala Shanmugam, Chunzi Huang, Melissa Gilbert‐Ross, Adam I. Marcus, Shagun Sharma, Gregory Joseph, Veronika Y Matsuk, Richa Sharma, Labdhi Mehta, An H Vu, Ticiana Leal, Melissa A Roy
article en
6 citations

Abstract

Non-small cell lung cancer (NSCLC) collective invasion is supported by cooperativity of proliferative (follower) and invasive (leader) cells. H1299-isolated follower cells exhibit higher Yes-associated protein (YAP) expression, while leader cells were found to express elevated transcriptional coactivator with PDZ-binding motif (TAZ/WWTR1) expression. Suppressing TAZ (not YAP) in leader cells reduced invasion. TAZ-regulated leader cell invasion is associated with activation of the EGFR-PI3K-AKT axis. NSCLC patient samples also demonstrated heterogeneity in YAP and TAZ expression. YAP and TAZ regulate proliferation of follower and leader cells. Our results highlight the need to inhibit both YAP and TAZ to effectively target their regulation of collective invasion. We identify that the SUMOylation inhibitor TAK-981 reduces YAP and TAZ expression, decreasing tumor burden and metastasis in a murine NSCLC model. Our study reveals an intra-tumoral division of labor, driven by differential YAP and TAZ expression, which can be effectively targeted with TAK-981 for NSCLC therapy.

iScienceVol. 27(11)
Emory University (US), Emory National Primate Research Center
Emory University, Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, Winship Cancer Institute, National Cancer Institute
Openalex Percentile: Top 15%
Hippo pathway signaling and YAP/TAZ
1.96
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