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Therapy-Induced Senescence Enhances the Efficacy of HER2-Targeted Antibody–Drug Conjugates in Breast Cancer
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Abstract
Antibody–drug conjugates (ADC) are antineoplastic agents recently introduced into the antitumor arsenal. T-DM1, a trastuzumab-based ADC that relies on lysosomal processing to release the payload, is approved for HER2-positive breast cancer. Next-generation ADCs targeting HER2, such as [vic-]trastuzumab duocarmazine (SYD985), bear linkers cleavable by lysosomal proteases and membrane-permeable drugs, mediating a bystander effect by which neighboring antigen-negative cells are eliminated. Many antitumor therapies, like DNA-damaging agents or CDK4/6 inhibitors, can induce senescence, a cellular state characterized by stable cell-cycle arrest. Another hallmark of cellular senescence is the enlargement of the lysosomal compartment. Given the relevance of the lysosome to the mechanism of action of ADCs, we hypothesized that therapies that induce senescence would potentiate the efficacy of HER2-targeting ADCs. Treatment with the DNA-damaging agent doxorubicin and CDK4/6 inhibitor induced lysosomal enlargement and senescence in several breast cancer cell lines. While senescence-inducing drugs did not increase the cytotoxic effect of ADCs on target cells, the bystander effect was enhanced when HER2-negative cells were cocultured with HER2-low cells. Knockdown experiments demonstrated the importance of cathepsin B in the enhanced bystander effect, suggesting that cathepsin B mediates linker cleavage. In breast cancer patient-derived xenografts, a combination treatment of CDK4/6 inhibitor and SYD985 showed improved antitumor effects over either treatment alone. These data support the strategy of combining next-generation ADCs targeting HER2 with senescence-inducing therapies for tumors with heterogenous and low HER2 expression. Significance: Combining ADCs against HER2-positive breast cancers with therapies that induce cellular senescence may improve their therapeutic efficacy by facilitating a bystander effect against antigen-negative tumor cells.
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References 35 · Cited by 45
Research works printed but not linked: 28
- Pegram, 2019, HER2-Overexpressing/amplified breast cancer as a testing ground for antibody-drug conjugate drug development in solid tumors, Clin Cancer Res, 26, 775, 10.1158/1078-0432.CCR-18-1976 · DOI
- Cortés, 2021, LBA1 trastuzumab deruxtecan (T-DXd) vs trastuzumab emtansine (T-DM1) in patients (Pts) with HER2+ metastatic breast cancer (mBC): results of the randomized phase III DESTINY-Breast03 study, Ann Oncol, 32, S1287, 10.1016/j.annonc.2021.08.2087 · DOI
- Cerami, 2012, The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data, Cancer Discov, 2, 401, 10.1158/2159-8290.CD-12-0095 · DOI · Paper page
- Phillips, 2008, Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate, Cancer Res, 68, 9280, 10.1158/0008-5472.CAN-08-1776 · DOI
- Erickson, 2006, Antibody-maytansinoid conjugates are activated in targeted cancer cells by lysosomal degradation and linker-dependent intracellular processing, Cancer Res, 66, 4426, 10.1158/0008-5472.CAN-05-4489 · DOI
- Manich, 2021, LBA15 primary outcome of the phase III SYD985.002/TULIP trial comparing [vic-]trastuzumab duocarmazine to physician's choice treatment in patients with pre-treated HER2-positive locally advanced or metastatic breast cancer, Ann Oncol, 32, S1288, 10.1016/j.annonc.2021.08.2088 · DOI
- van der Lee, 2015, The preclinical profile of the duocarmycin-based HER2-targeting ADC SYD985 predicts for clinical benefit in low HER2-expressing breast cancers, Mol Cancer Ther, 14, 692, 10.1158/1535-7163.MCT-14-0881-T · DOI
- Caculitan, 2017, Cathepsin B is dispensable for cellular processing of cathepsin B-cleavable antibody–drug conjugates, Cancer Res, 77, 7027, 10.1158/0008-5472.CAN-17-2391 · DOI
- Wang, 2020, Senescent cells in cancer therapy: friends or foes?, Trends Cancer, 6, 838, 10.1016/j.trecan.2020.05.004 · DOI · Paper page
- Robbins, 1970, Morphologic changes accompanying senescence of cultured human diploid cells, J Exp Med, 131, 1211, 10.1084/jem.131.6.1211 · DOI · Paper page
- Dimri, 1995, A biomarker that identifies senescent human cells in culture and in aging skin in vivo, Proc Natl Acad Sci U S A, 92, 9363, 10.1073/pnas.92.20.9363 · DOI · Paper page
- Lee, 2006, Senescence-associated β-galactosidase is lysosomal β-galactosidase, Aging Cell, 5, 187, 10.1111/j.1474-9726.2006.00199.x · DOI · Paper page
- Park, 2018, Adjustment of the lysosomal-mitochondrial axis for control of cellular senescence, Ageing Res Rev, 47, 176, 10.1016/j.arr.2018.08.003 · DOI · Paper page
- Angelini, 2013, Constitutive HER2 signaling promotes breast cancer metastasis through cellular senescence, Cancer Res, 73, 450, 10.1158/0008-5472.CAN-12-2301 · DOI
- Parra-Palau, 2014, Effect of p95HER2/611CTF on the response to trastuzumab and chemotherapy, J Natl Cancer Inst, 106, dju291, 10.1093/jnci/dju291 · DOI
- Nadal-Serrano, 2020, The second generation antibody-drug conjugate SYD985 overcomes resistances to T-DM1, Cancers, 12, 670, 10.3390/cancers12030670 · DOI
- Tarantino, 2020, HER2-low breast Cancer: pathological and clinical landscape, J Clin Oncol, 38, 1951, 10.1200/JCO.19.02488 · DOI
- Magnifico, 2009, Tumor-initiating cells of HER2-positive carcinoma cell lines express the highest oncoprotein levels and are sensitive to trastuzumab, Clin Cancer Res, 15, 2010, 10.1158/1078-0432.CCR-08-1327 · DOI
- Abdel-Latif, 2015, The chemomodulatory effects of resveratrol and didox on herceptin cytotoxicity in breast cancer cell lines, Sci Rep, 5, 12054, 10.1038/srep12054 · DOI
- Ríos-Luci, 2017, Resistance to the antibody-drug conjugate T-DM1 is based in a reduction in lysosomal proteolytic activity, Cancer Res, 77, 4639, 10.1158/0008-5472.CAN-16-3127 · DOI
- Sardiello, 2009, A gene network regulating lysosomal biogenesis and function, Science, 325, 473, 10.1126/science.1174447 · DOI · Paper page
- Doronina, 2003, Development of potent monoclonal antibody auristatin conjugates for cancer therapy, Nat Biotechnol, 21, 778, 10.1038/nbt832 · DOI
- Mijanović, 2019, Cathepsin B: a sellsword of cancer progression, Cancer Lett, 449, 207, 10.1016/j.canlet.2019.02.035 · DOI · Paper page
- Hu, 2015, Mechanistic investigation of bone marrow suppression associated with palbociclib and its differentiation from cytotoxic chemotherapies, Clin Cancer Res, 22, 2000, 10.1158/1078-0432.CCR-15-1421 · DOI
- Vijayaraghavan, 2017, CDK4/6 and autophagy inhibitors synergistically induce senescence in Rb positive cytoplasmic cyclin E negative cancers, Nat Commun, 8, 15916, 10.1038/ncomms15916 · DOI
- Modi, 2020, Antitumor activity and safety of trastuzumab deruxtecan in patients with HER2-low–expressing advanced breast Cancer: results from a phase Ib study, J Clin Oncol, 38, 10.1200/JCO.19.02318 · DOI
- Zhang, 2022, HER2-Low breast cancers, Am J Clin Pathol, 157, 328, 10.1093/ajcp/aqab117 · DOI
- 2020, Trastuzumab deruxtecan DESTINY for some cancers, Cancer Discov, 10, 898, 10.1158/2159-8290.CD-ND2020-011 · DOI
Metadata
- Authors
- Duro-Sánchez, S., Nadal-Serrano, M., Lalinde-Gutiérrez, M., Arenas, E. J., Bernadó Morales, C., Morancho, B., Escorihuela, M., Pérez-Ramos, S., Escrivá-de-Romaní, S., Gandullo-Sánchez, L., Pandiella, A., Esteve-Codina, A., Rodilla, V., Dijcks, F. A., Dokter, W. H. A., Cortés, J., Saura, C., & Arribas, J.
- Affiliations
- 1Preclinical and Translational Research Program, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
- Universitat Autònoma de Barcelona (ES)
- Centro de Investigación Biomédica en Red de Cáncer (ES)
- Vall d'Hebron Institute of Oncology (ES)
- Vall d'Hebron Hospital Universitari (ES)
- 2Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Barcelona, Spain.
- Centro de Investigación del Cáncer (ES)
- 7NAG-CRG, Centre for Genomic Regulation, Barcelona Institute of Science and Technology, Barcelona, Spain.
- Byondis BV (Netherlands) (NL)
- Hospital Del Mar (ES)
- ORCID
- Duro-Sánchez, Santiago
- Nadal-Serrano, Mercedes
- Lalinde-Gutiérrez, Marta
- Arenas, Enrique Javier
- Bernadó Morales, Cristina
- Morancho, Beatriz
- Escorihuela, Marta
- Pérez-Ramos, Sandra
- Escrivá-de-Romaní, Santiago
- Gandullo-Sánchez, Lucía
- Pandiella, Atanasio
- Esteve-Codina, Anna
- Rodilla, Verónica
- Dijcks, Fred A.
- Dokter, Wim H.A.
- Cortés, Javier
- Saura, Cristina
- Arribas, Joaquín
- Venue
- Cancer Research
- Published
- 2022-10-12
- Volume
- 82
- Issue
- 24
- Pages
- 4670-4679
- ISSN
- 0008-5472 (ISSN-L)
- 1538-7445
- PMC
- PMC9755966
- OpenAlex
- W4304694307
- Cited by
- 45
- References
- 35
- Citations by year
- 2026: 7 · 2025: 15 · 2024: 19 · 2023: 4
- FWCI
- 3.97
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Cancer Research (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Dipòsit Digital de Documents de la UAB (Universitat Autònoma de Barcelona) (submittedVersion, cc-by-nc-nd)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion, cc-by-nc-nd)
- Repositori digital de la UPF (Universitat Pompeu Fabra) (submittedVersion)
- Funders
- Breast Cancer Research Foundation (BCRF-20-008)
- Instituto de Salud Carlos III (AC15/00062, CB16/12/00449 and PI19/01181, PT17/0009/0019)
- Horizon 2020 Framework Programme (ERA-NET TRANSCAN-2)
- Fundación Mutua Madrileña
- Fundación Científica Asociación Española Contra el Cáncer
- Ministerio de Ciencia, Innovación y Universidades
- Topics
- Health Sciences › Medicine › Oncology › HER2/EGFR in Cancer Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Keywords
- therapy-induced senescence, HER2-targeted antibody-drug conjugates, bystander effect, lysosomal enlargement, cathepsin B, CDK4/6 inhibitors, doxorubicin, combination therapy, HER2-positive breast cancer, patient-derived xenografts
- MeSH terms
- Trastuzumab, Animals, Antineoplastic Agents, Breast Neoplasms, Cathepsin B, Female, Humans, Erb-b2 Receptor Tyrosine Kinases, Immunoconjugates, Xenograft Model Antitumor Assays, Cell Line, Tumor
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