Siegel R, Naishadham D, Jemal A. Cancer statistics, 2013. CA Cancer J Clin, 2013,63(1):11–30
PubMed
Article
Google Scholar
Jiang P, Enomoto A, Takahashi M. Cell biology of the movement of breast cancer cells: intracellular signaling and the actin cytoskeleton. Cancer Lett, 2009,284(2):122–130
PubMed
Article
CAS
Google Scholar
Graves P, Zeng Y. Biogenesis of mammalian microRNAs: a global view. Genomics Proteomics Bioinformatics, 2012,10(5):239–245
PubMed
Article
CAS
Google Scholar
Macfarlane LA, Murphy PR. MicroRNA: biogenesis, function and role in cancer. Curr Genomics, 2010,11(7):537–561
PubMed Central
PubMed
Article
CAS
Google Scholar
Burk U, Schubert J, Wellner U, et al. A reciprocal repression between ZEB1 and members of the miR-200 family promotes EMT and invasion in cancer cells. EMBO Rep, 2008,9(6):582–589
PubMed Central
PubMed
Article
CAS
Google Scholar
Peter ME. Let-7 and miR-200 microRNAs: guardians against pluripotency and cancer progression. Cell Cycle, 2009,8(6):843–852
PubMed Central
PubMed
Article
CAS
Google Scholar
Shimono Y, Zabala M, Cho RW, et al. Downregulation of miRNA-200c links breast cancer stem cells with normal stem cells. Cell, 2009,138(3):592–603
PubMed Central
PubMed
Article
CAS
Google Scholar
Schickel R, Park SM, Murmann AE, et al. mir-200c regulates induction of apoptosis through CD95 by targeting FAP-1. Mol Cell, 2010,38(6):908–915
PubMed Central
PubMed
Article
CAS
Google Scholar
Chang CJ, Chao CH, Xia W, et al. p53 regulates epithelial-mesenchymal transition and stem cell properties through modulating miRNAs. Nat Cell Biol, 2011,13(3):317–323
PubMed Central
PubMed
Article
CAS
Google Scholar
Cochrane DR, Spoelstra NS, Howe EN, et al. MicroRNA-200c mitigates invasiveness and restores sensitivity to microtubule-targeting chemotherapeutic agents. Mol Cancer Ther, 2009,8(5):1055–1066
PubMed
Article
CAS
Google Scholar
Lin J, Liu C, Gao F, et al. miR-200c enhances radiosensitivity of human breast cancer cells. J Cell Biochem, 2013,114(3):606–615
PubMed
Article
CAS
Google Scholar
Ahmad A, Aboukameel A, Kong D, et al. Phosphoglucose isomerase/autocrine motility factor mediates epithelial-mesenchymal transition regulated by miR-200 in breast cancer cells. Cancer Res, 2011,71(9):3400–3409
PubMed Central
PubMed
Article
CAS
Google Scholar
Howe EN, Cochrane DR, Cittelly DM, et al. miR-200c targets a NF-κB up-regulated TrkB/NTF3 autocrine signaling loop to enhance anoikis sensitivity in triple negative breast cancer. PLoS One, 2012,7(11):e49987
PubMed Central
PubMed
Article
CAS
Google Scholar
Jurmeister S, Baumann M, Balwierz A, et al. MicroRNA-200c represses migration and invasion of breast cancer cells by targeting actin-regulatory proteins FHOD1 and PPM1F. Mol Cell Biol, 2012,32(3):633–651
PubMed Central
PubMed
Article
CAS
Google Scholar
Chen Y, Sun Y, Chen L, et al. miRNA-200c increases the sensitivity of breast cancer cells to doxorubicin through the suppression of E-cadherin-mediated PTEN/Akt signaling. Mol Med Rep, 2013,7(5):1579–1584
PubMed
CAS
Google Scholar
Nikoletopoulou V, Markaki M, Palikaras K, et al. Crosstalk between apoptosis, necrosis and autophagy. Biochim Biophys Acta, 2013,1833(12):3448–3459
PubMed
Article
CAS
Google Scholar
Ko YB, Kim BR, Nam SL, et al. High-mobility group box 1 (HMGB1) protein regulates tumor-associated cell migration through the interaction with BTB domain. Cell Signal, 2014,26(4):777–783
PubMed
Article
CAS
Google Scholar
Tang D, Kang R, Zeh HJ 3rd, et al. High-mobility group box 1 and cancer. BBA, 2010,1799(1–2):131–140
PubMed Central
PubMed
CAS
Google Scholar
Sparatore B, Patrone M, Passalacqua M, et al. Activation of A431 human carcinoma cell motility by extracellular high-mobility group box 1 protein and epidermal growth factor stimuli. Biochem J, 2005,389(1):215–221
PubMed Central
PubMed
Article
CAS
Google Scholar
Brezniceanu ML, Völp K, Bösser S, et al. HMGB1 inhibits cell death in yeast and mammalian cells and is abundantly expressed in human breast carcinoma. FASEB J, 2003,17(10):1295–1297
PubMed
CAS
Google Scholar
Livesey KM, Kang R, Vernon P, et al. p53/HMGB1 complexes regulate autophagy and apoptosis. Cancer Res, 2012,72(8):1996–2005
PubMed Central
PubMed
Article
CAS
Google Scholar
van Beijnum JR, Nowak-Sliwinska P, van den Boezem E, et al. Tumor angiogenesis is enforced by autocrine regulation of high-mobility group box 1. Oncogene, 2013,32(3):363–374
PubMed
Article
CAS
Google Scholar
Jiao Y, Wang HC, Fan SJ. Growth suppression and radiosensitivity increase by HMGBI in breast cancer. Acta pharmacologica Sinica, 2007,28(12):1957–1967
PubMed
Article
CAS
Google Scholar
Bernardini M, Lee CH, Beheshti B, et a1. High-resolution mapping of genomic imbalance and identification of gene expression profiles associated with differential chemotherapy response in serous epithelial ovarian cancer. Neoplasia, 2005,7(6):603–613
PubMed Central
PubMed
Article
CAS
Google Scholar
Barnes KR, Kutikov A, Lippard SJ. Synthesis, characterization, and cytotoxicity of a series of estrogen-tethered platinum (IV) complexes. Chem Biol, 2004,11(4):557–564
PubMed
Article
CAS
Google Scholar
Gregory PA, Bracken CP, Smith E, et al. An autocrine TGF-beta/ZEB/miR-200 signaling network regulates establishment and maintenance of epithelial-mesenchymal transition. Mol Biol Cell, 2011,22(10):1686–1698
PubMed Central
PubMed
Article
CAS
Google Scholar
Tobar N, Villar V, Santibanez JF. ROS-NFkappaB mediates TGF-beta1-induced expression of urokinase-type plasminogen activator, matrix metalloproteinase-9 and cell invasion. Mol Cell Biochem, 2010,340(1–2):195–202
PubMed
Article
CAS
Google Scholar
Chua HL, Bhat-Nakshatri P, Clare SE. NF-kappaB represses E-cadherin expression and enhances epithelial to mesenchymal transition of mammary epithelial cells: potential involvement of ZEB-1 and ZEB-2. Oncogene, 2007,26(5):711–724
PubMed
Article
CAS
Google Scholar
Wu X, Mi Y, Yang H, et al. The activation of HMGB 1 as a progression factor on inflammation response in normal human bronchial epithelial cells through RAGE/JNK/NF-κB pathway, Mol Cell Biochem, 2013,380(1–2):249–257
PubMed
Article
CAS
Google Scholar
Smolarczyk R, Cichoń T, Jarosz M, et al. HMGB1—its role in tumor progression and anticancer therapy. Postepy Hig Med Dosw, 2012,22(66):913–920
Article
Google Scholar