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Suppl Figure 1-6, Suppl Table S0 and Suppl Methods from A Unique Morphological Phenotype in Chemoresistant Triple-Negative Breast Cancer Reveals Metabolic Reprogramming and PLIN4 Expression as a Molecular Vulnerability

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posted on 2023-04-03, 17:25 authored by Isabelle Sirois, Adriana Aguilar-Mahecha, Josiane Lafleur, Emma Fowler, Viet Vu, Michelle Scriver, Marguerite Buchanan, Catherine Chabot, Aparna Ramanathan, Banujan Balachandran, Stéphanie Légaré, Ewa Przybytkowski, Cathy Lan, Urszula Krzemien, Luca Cavallone, Olga Aleynikova, Cristiano Ferrario, Marie-Christine Guilbert, Naciba Benlimame, Amine Saad, Moulay Alaoui-Jamali, Horace Uri Saragovi, Sylvia Josephy, Ciara O'Flanagan, Stephen D. Hursting, Vincent R. Richard, René P. Zahedi, Christoph H. Borchers, Eric Bareke, Sheida Nabavi, Peter Tonellato, Josée-Anne Roy, André Robidoux, Elizabeth A. Marcus, Catalin Mihalcioiu, Jacek Majewski, Mark Basik

Supplementary Figure 1 a. Doxorubicin resistance of DOXO-R C8 cells was further validated using the cell viability assay (SRB) following 48 hrs treatment with DOXO, n=4 independent experiment, 3 replicates/experiment. **p<0.01 vs parental. b DOXO-R cells are not cross resistant to cisplatin. Cell viability measured by alamar blue following treatment with cisplatin for 48hrs, n=4 independent experiment, 3 replicates/experiment. c ABCB1 mRNA levels are not increased in DOXO-R cells compared to parental cells. Gene expression data showing LOG2FC values of C1, C8, CD and CF colonies compared to parental cells for ABCB1 gene. LOG2FC do not reach significance, i.e. LOG2FC >0.6 and pval<0.05. d DOXO-R cells do not express more ALDH+ve cells than parental cells. % of ALDH+ve cells quantified by flow cytometry, n=3 independent experiments, *p<0.05 vs parental. e Doubling time (hrs) of parental (P) and DOXO-R C1 and C8 cells measured by alamar blue, n=4 independent experiment, 3 replicates/experiment. *p<0.05 vs parental, n.s. = not significant. f Light microscopy of parental PTX selected colonies (PTX-CD and PTX-CF) showing that PTX colonies are different from parental cells but similar to DOXO-R C1 and C8 with neuron-like projections described in Fig. 2a. g Electron micrographs of PTX-CD and CF cells showing increased LDs (left panel, arrows), neuron-like projections (middle panel, arrow heads) and cytoplasmic regions filled with numerous small mitochondria (right panel, white circles), similar to DOXO-R C1 and C8 cells described in Fig. 2a. h Phalloidin staining showing PTX-CF cells but not parental cells exhibit PGCCs with neuron-like projections as shown in DOXO-R C1 and C8 cells in Fig. 2b. Scale bars 10, 5 and 2 µm. For a-d, data represent means +/- SEM. Student t-test was done for c-e. For a and b, two-way anova analysis with multiple comparison test (Dunnet) was performed. Supplementary Figure 2. Example of DOXO-R PGCC with neuron-like projection at high cell confluence visible by light microscopy at lower magnification (4x). Supplementary Figure 3. Omics analysis of chemoresistant TNBC cells and tumors. Supplementary Figure 4. a,b PPARG and PLIN4 mRNA quantification by RT-PCR following transient silencing of PPARG using 2 siRNAs (2 and 5) and siRNA ctrl in DOXO-R cells (n=3 independent experiment, *p<0.05, **p<0.01). Supplementary Figure 5. KM plots. Supplementary Figure 6. a,b Cell viability of MDA-MB-436 and CRC T786 (5000 cells/well) measured by alamar blue following treatment with DOXO in F-medium for 72hrs (n{greater than or equal to}3). Supplementary Table S0. Summary of the molecular characteristics identifying the DOXO-R phenotype in chemoresistant TNBC cells and tumors.

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FRQS

Canadian Research Society

Canadian Institutes of Health Research

Bourse de recherche en cancer du sein

McGill

GTP

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ARTICLE ABSTRACT

The major obstacle in successfully treating triple-negative breast cancer (TNBC) is resistance to cytotoxic chemotherapy, the mainstay of treatment in this disease. Previous preclinical models of chemoresistance in TNBC have suffered from a lack of clinical relevance. Using a single high dose chemotherapy treatment, we developed a novel MDA-MB-436 cell-based model of chemoresistance characterized by a unique and complex morphologic phenotype, which consists of polyploid giant cancer cells giving rise to neuron-like mononuclear daughter cells filled with smaller but functional mitochondria and numerous lipid droplets. This resistant phenotype is associated with metabolic reprogramming with a shift to a greater dependence on fatty acids and oxidative phosphorylation. We validated both the molecular and histologic features of this model in a clinical cohort of primary chemoresistant TNBCs and identified several metabolic vulnerabilities including a dependence on PLIN4, a perilipin coating the observed lipid droplets, expressed both in the TNBC-resistant cells and clinical chemoresistant tumors treated with neoadjuvant doxorubicin-based chemotherapy. These findings thus reveal a novel mechanism of chemotherapy resistance that has therapeutic implications in the treatment of drug-resistant cancer. These findings underlie the importance of a novel morphologic–metabolic phenotype associated with chemotherapy resistance in TNBC, and bring to light novel therapeutic targets resulting from vulnerabilities in this phenotype, including the expression of PLIN4 essential for stabilizing lipid droplets in resistant cells.

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