Abstract
Abstract 2248: Paclitaxel-induced micronucleation activates pro-inflammatory cGAS/STING signaling in triple negative breast cancer
Cancer research (Chicago, Ill.), Vol.80(16_Supplement), pp.2248-2248
08/15/2020
DOI: 10.1158/1538-7445.AM2020-2248
Abstract
Abstract
Introduction: Paclitaxel (TaxolTM) is a blockbuster chemotherapy used for solid tumors including breast cancer. In triple-negative breast cancer (TNBC), nab-paclitaxel plus PD-L1 inhibitor, atezolizumab, is now approved based on increased survival compared with nab-paclitaxel alone. We hypothesize that there may be an interaction by which taxane therapy is immunogenic. Paclitaxel induces aberrant cell division on multipolar spindles, which often results in formation of multiple small nuclei. Some of these resemble micronuclei. Here, we test the hypothesis that taxane-induced micronuclei activate cGAS-STING to increase immunogenicity in TNBC.
Methods: We evaluate the impact of clinically relevant doses of paclitaxel on TNBC cell lines MDA-MB-231, MDA-MB-453, MDA-MB-468, BT-549 and HCC-1806 on generating micronuclei by immunofluorescence microscopy. Using immunoblotting and qPCR, we evaluate the impact of paclitaxel on cGAS recruitment and activation, STING activation, and interferon-beta production. Furthermore, we co-culture MDA-MB-231 and THP-1 cells to evaluate the impact of paclitaxel on polarization of THP-1 macrophages. We employ CRISPR-mediated cGAS knockout to evaluate its role in mediating these effects. Finally, we test the effect of neoadjuvant paclitaxel (80 mg/m2 qw, 16 treatments/4 cycles) in 4 patients for formation of micronuclei and tumor-infiltrating lymphocytes 20 hours after the third treatment of paclitaxel by H&E.
Results: We observe that post-mitotic cells often contain micronuclei. cGAS recruitment is detected in some micronuclei, more commonly in multinucleated cells. With three days of paclitaxel, the cGAS-positive cell population increases from 9% (+/- 1.3) to 34% (+/- 2.4) in MDA-MB-231. Similar trends are observed in other cell lines. In MDA-MB-231 cells, synthesis of 2'3'-cGAMP and IFN-beta is increased after paclitaxel. Upregulation of interferon stimulated genes and phospho-proteins also supports STING activation, which is abolished in cGAS knockout cells. Co-culture of THP-1 macrophages with MDA-MB-231 cells in paclitaxel, or conditioned media from MDA-MB-231 cells pre-treated with paclitaxel, polarizes THP-1 cells from an M0 to M1 phenotype. Furthermore, we observe an increase in micronuclei and TILs after paclitaxel for 3 of 4 patient samples with one patient converting from a plasma cell-rich to a lymphocyte-rich infiltrate.
Conclusions: Physiologic levels of paclitaxel can generate micronuclei to activate the cGAS-STING pathway in breast cancer cell lines and to induce a pro-inflammatory interferon-beta driven response. This may present a post-mitotic mechanism for paclitaxel-mediated cancer cell death. These data may provide the mechanistic basis for the high efficacy seen in combining taxanes with immunotherapies.
Citation Format: Yang Hu, Ning Jin, Baraa K. Manasrah, Stephanie M. McGregor, Christina Scribano, John B. Tucker, Rachel Yan, Robert F. Lera, Beth A. Weaver, Mark E. Burkard. Paclitaxel-induced micronucleation activates pro-inflammatory cGAS/STING signaling in triple negative breast cancer [abstract]. In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24. Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr 2248.
Details
- Title: Subtitle
- Abstract 2248: Paclitaxel-induced micronucleation activates pro-inflammatory cGAS/STING signaling in triple negative breast cancer
- Creators
- Yang Hu - University of Wisconsin–MadisonNing Jin - Ohio UniversityBaraa K. Manasrah - University of Wisconsin–MadisonStephanie M. McGregor - University of Wisconsin–MadisonChristina Scribano - University of Wisconsin–MadisonJohn B. Tucker - University of Wisconsin–MadisonRachel Yan - University of Wisconsin–MadisonRobert F. Lera - University of Wisconsin–MadisonBeth A. Weaver - University of Wisconsin–MadisonMark E. Burkard - University of Wisconsin–Madison
- Resource Type
- Abstract
- Publication Details
- Cancer research (Chicago, Ill.), Vol.80(16_Supplement), pp.2248-2248
- Publisher
- AMER ASSOC CANCER RESEARCH; PHILADELPHIA
- DOI
- 10.1158/1538-7445.AM2020-2248
- ISSN
- 0008-5472
- eISSN
- 1538-7445
- Language
- English
- Date published
- 08/15/2020
- Academic Unit
- Internal Medicine
- Record Identifier
- 9984700647402771
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