W. Berg, D. Cosgrove, C. Doré, F. Schäfer, W. Svensson et al., Shear-wave Elastography Improves the Specificity of Breast US: The BE1 Multinational Study of 939 Masses, Radiology, vol.262, issue.2, pp.435-484, 2012.
DOI : 10.1148/radiol.11110640

K. Pepin, R. Ehman, and K. Mcgee, Magnetic resonance elastography (MRE) in cancer: Technique, analysis, and applications, Progress in Nuclear Magnetic Resonance Spectroscopy, vol.90, issue.91, pp.90-91, 2015.
DOI : 10.1016/j.pnmrs.2015.06.001
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660259

I. Acerbi, L. Cassereau, I. Dean, Q. Shi, A. Au et al., Human breast cancer invasion and aggression correlates with ECM stiffening and immune cell infiltration, Integr. Biol., vol.27, issue.1, pp.1120-1154, 2015.
DOI : 10.1101/cshperspect.a005058
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593730

J. Mouw, Y. Yui, L. Damiano, R. Bainer, J. Lakins et al., Tissue mechanics modulate microRNA-dependent PTEN expression to regulate malignant progression, Nature Medicine, vol.31, issue.4, pp.360-367, 2014.
DOI : 10.1038/nm.3497
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981899

V. Seewaldt, ECM stiffness paves the way for tumor cells, Nature Medicine, vol.20, issue.4, pp.332-335, 2014.
DOI : 10.1172/JCI39534

A. Minchinton and I. Tannock, Drug penetration in solid tumours, Nature Reviews Cancer, vol.23, issue.1, pp.583-92, 2006.
DOI : 10.1038/nrc1893

R. Jain and T. Stylianopoulos, Delivering nanomedicine to solid tumors, Nature Reviews Clinical Oncology, vol.3, issue.11, pp.653-64, 2010.
DOI : 10.1038/nrclinonc.2010.139
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065247

S. Torosean, B. Flynn, J. Axelsson, J. Gunn, K. Samkoe et al., Nanoparticle uptake in tumors is mediated by the interplay of vascular and collagen density with interstitial pressure, Nanomedicine: Nanotechnology, Biology and Medicine, vol.9, issue.2, pp.151-159, 2012.
DOI : 10.1016/j.nano.2012.07.002

P. Provenzano, C. Cuevas, A. Chang, V. Goel, V. Hoff et al., Enzymatic Targeting of the Stroma Ablates Physical Barriers to Treatment of Pancreatic Ductal Adenocarcinoma, Cancer Cell, vol.21, issue.3, pp.418-447, 2012.
DOI : 10.1016/j.ccr.2012.01.007

B. Diop-frimpong, V. Chauhan, S. Krane, Y. Boucher, and R. Jain, Losartan inhibits collagen I synthesis and improves the distribution and efficacy of nanotherapeutics in tumors, Proceedings of the National Academy of Sciences, vol.108, issue.7, pp.2909-2923, 2011.
DOI : 10.1073/pnas.1018892108

C. Wong, T. Stylianopoulos, J. Cui, J. Martin, V. Chauhan et al., Multistage nanoparticle delivery system for deep penetration into tumor tissue, Proceedings of the National Academy of Sciences, vol.108, issue.6, pp.2426-2457, 2011.
DOI : 10.1073/pnas.1018382108
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038705

P. Netti, D. Berk, M. Swartz, A. Grodzinsky, and R. Jain, Role of extracellular matrix assembly in interstitial transport in solid tumors, Cancer Res, vol.60, pp.2497-503, 2000.

W. Mok, Y. Boucher, and R. Jain, Matrix Metalloproteinases-1 and -8 Improve the Distribution and Efficacy of an Oncolytic Virus, Cancer Research, vol.67, issue.22, pp.10664-10672, 2007.
DOI : 10.1158/0008-5472.CAN-07-3107

G. Alexandrakis, E. Brown, R. Tong, T. Mckee, R. Campbell et al., Two-photon fluorescence correlation microscopy reveals the two-phase nature of transport in tumors, Nature Medicine, vol.10, issue.2, pp.203-210, 2004.
DOI : 10.1038/nm981

R. Singh and S. Torti, Carbon nanotubes in hyperthermia therapy, Advanced Drug Delivery Reviews, vol.65, issue.15, pp.2045-60, 2013.
DOI : 10.1016/j.addr.2013.08.001

K. Sano, T. Nakajima, P. Choyke, and H. Kobayashi, Markedly Enhanced Permeability and Retention Effects Induced by Photo-immunotherapy of Tumors, ACS Nano, vol.7, issue.1, pp.717-741, 2012.
DOI : 10.1021/nn305011p

A. Bagley, R. Scherz-shouval, P. Galie, A. Zhang, J. Wyckoff et al., Endothelial Thermotolerance Impairs Nanoparticle Transport in Tumors, Cancer Research, vol.75, issue.16, pp.3255-67, 2015.
DOI : 10.1158/0008-5472.CAN-15-0325
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833008

J. Kolosnjaj-tabi, D. Corato, R. Lartigue, L. Marangon, I. Guardia et al., Heat-Generating Iron Oxide Nanocubes: Subtle ???Destructurators??? of the Tumoral Microenvironment, ACS Nano, vol.8, issue.5, pp.4268-83, 2014.
DOI : 10.1021/nn405356r

J. Lo, G. Von-maltzahn, J. Douglass, J. Park, M. Sailor et al., Nanoparticle amplification via photothermal unveiling of cryptic collagen binding sites, Journal of Materials Chemistry B, vol.177, issue.39, pp.5235-5275, 2013.
DOI : 10.1039/c3tb20619j

S. Sapareto and W. Dewey, Thermal dose determination in cancer therapy, International Journal of Radiation Oncology*Biology*Physics, vol.10, issue.6, pp.787-800, 1984.
DOI : 10.1016/0360-3016(84)90379-1

F. Chamming-'s, H. Latorre-ossa, L. Frère-belda, M. Fitoussi, V. Quibel et al., Shear wave elastography of tumour growth in a human breast cancer model with pathological correlation, European Radiology, vol.57, issue.8, pp.2079-86, 2013.
DOI : 10.1007/s00330-013-2828-8

S. Lee, W. Moon, N. Cho, J. Chang, H. Moon et al., Shear-Wave Elastographic Features of Breast Cancers, Investigative Radiology, vol.49, issue.3, pp.147-55, 2014.
DOI : 10.1097/RLI.0000000000000006

A. Athanasiou, H. Latorre-ossa, A. Criton, A. Tardivon, J. Gennisson et al., Feasibility of Imaging and Treatment Monitoring of Breast Lesions with Three-Dimensional Shear Wave Elastography, Ultraschall in der Medizin - European Journal of Ultrasound, vol.38, issue.01, pp.10-1055, 2015.
DOI : 10.1055/s-0034-1398980

A. Mariani, W. Kwiecinski, M. Pernot, D. Balvay, M. Tanter et al., Real time shear waves elastography monitoring of thermal ablation: in??vivo evaluation in pig livers, Journal of Surgical Research, vol.188, issue.1, pp.37-43, 2014.
DOI : 10.1016/j.jss.2013.12.024

W. Kwiecinski, F. Bessière, E. Constanciel, N. Djin, W. Tanter et al., Cardiac shear-wave elastography using a transesophageal transducer: application to the mapping of thermal lesions in ultrasound transesophageal cardiac ablation, Physics in Medicine and Biology, vol.60, issue.20, pp.7829-7875, 2015.
DOI : 10.1088/0031-9155/60/20/7829

E. Sapin-de-brosses, J. Gennisson, M. Pernot, M. Fink, and M. Tanter, Temperature dependence of the shear modulus of soft tissues assessed by ultrasound, Physics in Medicine and Biology, vol.55, issue.6, pp.1701-1719, 2010.
DOI : 10.1088/0031-9155/55/6/011

E. Brown, T. Mckee, E. Pluen, A. Seed, B. Boucher et al., Dynamic imaging of collagen and its modulation in tumors in vivo using second-harmonic generation, Nature Medicine, vol.9, issue.6, pp.796-800, 2003.
DOI : 10.1038/nm879

V. Shanmugam, S. Selvakumar, and C. Yeh, Near-infrared light-responsive nanomaterials in cancer therapeutics, Chemical Society Reviews, vol.8, issue.17, pp.6254-87, 2014.
DOI : 10.2217/nnm.13.84

J. Melamed, R. Edelstein, and E. Day, Elucidating the Fundamental Mechanisms of Cell Death Triggered by Photothermal Therapy, ACS Nano, vol.9, issue.1, pp.6-11, 2015.
DOI : 10.1021/acsnano.5b00021

M. Pérez-hernández, P. Del-pino, S. Mitchell, M. Moros, G. Stepien et al., Dissecting the Molecular Mechanism of Apoptosis during Photothermal Therapy Using Gold Nanoprisms, ACS Nano, vol.9, issue.1, pp.52-61, 2015.
DOI : 10.1021/nn505468v

I. Marangon, C. Ménard-moyon, A. Silva, A. Bianco, N. Luciani et al., Synergic mechanisms of photothermal and photodynamic therapies mediated by photosensitizer/carbon nanotube complexes, Carbon, vol.97, pp.110-133, 2016.
DOI : 10.1016/j.carbon.2015.08.023

L. Miao, C. Lin, and L. Huang, Stromal barriers and strategies for the delivery of nanomedicine to desmoplastic tumors, Journal of Controlled Release, vol.219, pp.192-204, 2015.
DOI : 10.1016/j.jconrel.2015.08.017

I. Khawar, J. Kim, and H. Kuh, Improving drug delivery to solid tumors: Priming the tumor microenvironment, Journal of Controlled Release, vol.201, pp.78-89, 2015.
DOI : 10.1016/j.jconrel.2014.12.018

H. Liang, X. Li, C. B. Wang, B. Zhao, Y. Zhuang et al., A collagen-binding EGFR single-chain Fv antibody fragment for the targeted cancer therapy, Journal of Controlled Release, vol.209, pp.101-110, 2015.
DOI : 10.1016/j.jconrel.2015.04.029

T. Wu, J. Felmlee, J. Greenleaf, S. Riederer, and R. Ehman, Assessment of thermal tissue ablation with MR elastography, Magnetic Resonance in Medicine, vol.10, issue.1, pp.80-87, 2001.
DOI : 10.1002/1522-2594(200101)45:1<80::AID-MRM1012>3.0.CO;2-Y

J. Chen, D. Woodrum, K. Glaser, M. Murphy, K. Gorny et al., Assessment of in vivo laser ablation using MR elastography with an inertial driver, Magnetic Resonance in Medicine, vol.55, issue.1, pp.59-67, 2014.
DOI : 10.1002/mrm.24891

P. Yarmolenko, E. Moon, C. Landon, A. Manzoor, D. Hochman et al., Thresholds for thermal damage to normal tissues: An update, International Journal of Hyperthermia, vol.1107, issue.2, pp.320-363, 2011.
DOI : 10.1080/0265673042000209770
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3609720

I. Marangon, C. Ménard-moyon, J. Kolosnjaj-tabi, M. Béoutis, L. Lartigue et al., Covalent Functionalization of Multi-walled Carbon Nanotubes with a Gadolinium Chelate for Efficient T1-Weighted Magnetic Resonance Imaging, Adv Funct Mater, vol.24, pp.7173-86, 2014.