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Non-Canonical Activin A Signaling Stimulates Context-Dependent and Cellular-Specific Outcomes in CRC to Promote Tumor Cell Migration and Immune Tolerance.
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- Author(s): Wiley, Mark B.; Bauer, Jessica; Mehrotra, Kunaal; Zessner-Spitzenberg, Jasmin; Kolics, Zoe; Cheng, Wenxuan; Castellanos, Karla; Nash, Michael G.; Gui, Xianyong; Kone, Lyonell; Maker, Ajay V.; Qiao, Guilin; Reddi, Deepti; Church, David N.; Kerr, Rachel S.; Kerr, David J.; Grippo, Paul J.; Jung, Barbara
- Source:
Cancers; Jun2023, Vol. 15 Issue 11, p3003, 19p- Subject Terms:
- Source:
- Additional Information
- Abstract: Simple Summary: The identification of markers of metastatic disease is critical to improving colorectal cancer survival rates. Activin A plays a critical role in tumor and immune cells in colorectal cancer. Here, we aimed to expand on our previous work to determine how activin A influences tumor cell signaling and immune activation status. Our findings suggest that activin A inhibits the activity of immune cells found in the tumors of colorectal cancer patients while promoting metastasis. Furthermore, we provide data suggesting activin A stimulates a targetable pathway in tumor cells and immune cells leading to metastatic outcomes. This work highlights the application of novel, commercially available imaging techniques to colorectal cancer patient samples to confirm signaling networks driving disease progression. The identification of activin-induced pathways driving metastasis may provide an early target for colorectal cancer to inhibit progression. We have shown that activin A (activin), a TGF-β superfamily member, has pro-metastatic effects in colorectal cancer (CRC). In lung cancer, activin activates pro-metastatic pathways to enhance tumor cell survival and migration while augmenting CD4+ to CD8+ communications to promote cytotoxicity. Here, we hypothesized that activin exerts cell-specific effects in the tumor microenvironment (TME) of CRC to promote anti-tumoral activity of immune cells and the pro-metastatic behavior of tumor cells in a cell-specific and context-dependent manner. We generated an Smad4 epithelial cell specific knockout (Smad4−/−) which was crossed with TS4-Cre mice to identify SMAD-specific changes in CRC. We also performed IHC and digital spatial profiling (DSP) of tissue microarrays (TMAs) obtained from 1055 stage II and III CRC patients in the QUASAR 2 clinical trial. We transfected the CRC cells to reduce their activin production and injected them into mice with intermittent tumor measurements to determine how cancer-derived activin alters tumor growth in vivo. In vivo, Smad4−/− mice displayed elevated colonic activin and pAKT expression and increased mortality. IHC analysis of the TMA samples revealed increased activin was required for TGF-β-associated improved outcomes in CRC. DSP analysis identified that activin co-localization in the stroma was coupled with increases in T-cell exhaustion markers, activation markers of antigen presenting cells (APCs), and effectors of the PI3K/AKT pathway. Activin-stimulated PI3K-dependent CRC transwell migration, and the in vivo loss of activin lead to smaller CRC tumors. Taken together, activin is a targetable, highly context-dependent molecule with effects on CRC growth, migration, and TME immune plasticity. [ABSTRACT FROM AUTHOR]
- Abstract: Copyright of Cancers is the property of MDPI and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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