13058_2021_1390_MOESM1_ESM.docx (280.08 kB)
Download fileAdditional file 1 of RANK signaling increases after anti-HER2 therapy contributing to the emergence of resistance in HER2-positive breast cancer
journal contribution
posted on 2021-03-31, 03:43 authored by Adrián Sanz-Moreno, Sonia Palomeras, Kim Pedersen, Beatriz Morancho, Tomas Pascual, Patricia Galván, Sandra Benítez, Jorge Gomez-Miragaya, Marina Ciscar, Maria Jimenez, Sonia Pernas, Anna Petit, María Teresa Soler-Monsó, Gemma Viñas, Mansour Alsaleem, Emad A. Rakha, Andrew R. Green, Patricia G. Santamaria, Celine Mulder, Simone Lemeer, Joaquin Arribas, Aleix Prat, Teresa Puig, Eva Gonzalez-SuarezAdditional file 1: Figure S1. TMA H-scores and controls. A. RANK and RANKL H-scores in HER2-positive breast cancer samples, treatment-naïve (left panels) or anti-HER2-resistant (right panels). In treatment-naïve TMAs, each number represents a “core” from a single patient. In anti-HER2-resistant TMAs, scored independent tumor cores are numbered for each patient (after the symbol #). B. Representative pictures of human breast tumors from patient-derived xenografts used as positive and negative controls for RANK and RANKL IHC.
Funding
Fundació la Marató de TV3 (ES) Ministerio de Ciencia, Innovación y Universidades Susan G. Komen Instituto de Salud Carlos III Breast Cancer Research Foundation (US) European Research Council Fundación Científica Asociación Española Contra el Cáncer
History
References
- 10.1038/sj.onc.1210477
- 10.1126/science.3798106
- 10.1177/1758835919833519
- 10.1200/JCO.19.00443
- 10.1056/NEJMoa1814017
- 10.1038/s41467-019-14111-3
- 10.1038/nrd3705
- 10.1158/0008-5472.CAN-15-2745
- 10.1038/nature09495
- 10.1038/nature09387
- 10.1158/0008-5472.CAN-12-0044
- 10.1007/s10549-014-2955-1
- 10.1038/nm.4118
- 10.1038/cr.2016.69
- 10.1038/nature09707
- 10.1016/j.clbc.2017.05.011
- 10.1016/j.critrevonc.2019.05.001
- 10.1002/ijc.21004
- 10.1007/s10549-012-2149-7
- 10.1016/S1470-2045(17)30021-9
- 10.1200/JCO.2008.18.1370
- 10.1001/jamaoncol.2016.0922
- 10.1038/s41467-020-20138-8
- 10.1128/MCB.01298-06
- 10.1158/0008-5472.CAN-16-2976
- 10.1371/journal.pone.0131241
- 10.1038/onc.2012.152
- 10.1158/0008-5472.CAN-10-1701
- 10.1186/s13058-015-0538-7
- 10.1371/journal.pone.0019234
- 10.1158/0008-5472.CAN-08-4490
- 10.1038/sj.onc.1203239
- 10.1111/gtc.12012
- 10.1016/j.bbrc.2018.09.086
- 10.1016/j.celrep.2019.11.008
- 10.1007/s10549-019-05489-1
- 10.1016/j.ccr.2014.02.025
- 10.1158/0008-5472.CAN-06-3409
- 10.1002/jcp.21511
- 10.1038/s41388-018-0324-y
- 10.1016/j.molmed.2016.07.009
- 10.1186/s13058-019-1226-9
- 10.2353/ajpath.2009.080706
- 10.1158/0008-5472.CAN-10-0732
- 10.1038/36593
- 10.1158/1541-7786.MCR-13-0206-T
- 10.1186/bcr3575
- 10.1177/1010428317706919
- 10.18632/oncoscience.18
- 10.2174/0929867321666141106124315
- 10.1101/cshperspect.a000158
- 10.1038/onc.2009.410
- 10.1016/S0092-8674(01)00599-2
- 10.3892/ol.2011.487