Skip to main content
Erschienen in: Cellular Oncology 4/2020

14.04.2020 | Original paper

Effect of EphA2 knockdown on melanoma metastasis depends on intrinsic ephrinA1 level

verfasst von: Jing Mo, Xiulan Zhao, Xueyi Dong, Tieju Liu, Nan Zhao, Danfang Zhang, Wei Wang, Yanhui Zhang, Baocun Sun

Erschienen in: Cellular Oncology | Ausgabe 4/2020

Einloggen, um Zugang zu erhalten

Abstract

Purpose

Upregulation of receptor tyrosine kinase EphA2 has been found to be associated with a poor prognosis in many types of cancer and is considered an attractive therapeutic target. As yet, few efforts have been focused on its tumor suppressive activity triggered by its ligand, ephrinA1. Here, we aimed to determine the potential of ephrinA1 as an important player in melanoma metastasis.

Methods

Data from the Cancer Genome Atlas (TCGA) and the Cancer Cell Line Encyclopedia (CCLE) were analyzed to explore the expression and prognostic implications of EphA2 and ephrinA1 in melanoma. Western blotting, shRNA, colony formation and immunofluorescence assays, as well as two in vivo xenograft models (subcutaneous and metastatic) were used to evaluate the role of EphA2 in melanoma progression. Akt inhibition and ephrinA1-Fc were used to confirm the influence of Akt activation and ephrinA1 levels on the EphA2 effects. Immunohistochemistry (IHC) was performed on xenograft and patient melanoma tissues.

Results

We found that high levels of ephrinA1, but not EphA2, were negatively correlated with melanoma metastasis. The expression levels of EphA2 and ephrinA1 were not correlated. After EphA2 downregulation, colony forming abilities and lung metastatic growth were reduced in melanoma cell lines with a low ephrinA1 expression, but were increased in melanoma cell lines with a high ephrinA1 expression. EphA2-mediated colony formation in EphA2-high/ephrinA1-low cells was found to be Akt-dependent and to be inhibited by the addition of ephrinA1-Fc. IHC staining of primary melanoma specimens revealed that EphA2-high/ephrinA1-low patients exhibited poorer outcomes than EphA2-high/ephrinA1-high patients.

Conclusions

From our data we conclude that evaluation of ephrinA1 levels may be helpful for the application of EphA2-targeted therapies and for prognostic predictions in melanoma patients.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat C.M. Balch, S.J. Soong, M.B. Atkins, A.C. Buzaid, N. Cascinelli, D.G. Coit, I.D. Fleming, J.E. Gershenwald, A. Houghton Jr., J.M. Kirkwood, K.M. McMasters, M.F. Mihm, D.L. Morton, D.S. Reintgen, M.I. Ross, A. Sober, J.A. Thompson, J.F. Thompson, An evidence-based staging system for cutaneous melanoma. CA Cancer J. Clin. 54(3), 131–149 (2004) quiz 182 – 134PubMedCrossRef C.M. Balch, S.J. Soong, M.B. Atkins, A.C. Buzaid, N. Cascinelli, D.G. Coit, I.D. Fleming, J.E. Gershenwald, A. Houghton Jr., J.M. Kirkwood, K.M. McMasters, M.F. Mihm, D.L. Morton, D.S. Reintgen, M.I. Ross, A. Sober, J.A. Thompson, J.F. Thompson, An evidence-based staging system for cutaneous melanoma. CA Cancer J. Clin. 54(3), 131–149 (2004) quiz 182 – 134PubMedCrossRef
2.
Zurück zum Zitat S.P. Leong, J.E. Gershenwald, S.J. Soong, D. Schadendorf, A.A. Tarhini, S. Agarwala, A. Hauschild, C.W. Soon, A. Daud, M. Kashani-Sabet, Cutaneous melanoma: a model to study cancer metastasis. J Surg Oncol 103(6), 538–549; (2011)PubMedCrossRef S.P. Leong, J.E. Gershenwald, S.J. Soong, D. Schadendorf, A.A. Tarhini, S. Agarwala, A. Hauschild, C.W. Soon, A. Daud, M. Kashani-Sabet, Cutaneous melanoma: a model to study cancer metastasis. J Surg Oncol 103(6), 538–549; (2011)PubMedCrossRef
3.
Zurück zum Zitat E.B. Pasquale, Eph-ephrin bidirectional signaling in physiology and disease. Cell 133(1), 38–52 (2008)PubMedCrossRef E.B. Pasquale, Eph-ephrin bidirectional signaling in physiology and disease. Cell 133(1), 38–52 (2008)PubMedCrossRef
4.
Zurück zum Zitat T.T. Ma, L. Wang, J.L. Wang, Y.J. Liu, Y.C. Chen, H.J. He, Y. Song, Hypoxia-Induced cleavage of soluble ephrinA1 from cancer cells is mediated by MMP-2 and associates with angiogenesis in oral squamous cell carcinoma. OncoTargets Therapy 12, 8491–8499 (2019)PubMedCrossRef T.T. Ma, L. Wang, J.L. Wang, Y.J. Liu, Y.C. Chen, H.J. He, Y. Song, Hypoxia-Induced cleavage of soluble ephrinA1 from cancer cells is mediated by MMP-2 and associates with angiogenesis in oral squamous cell carcinoma. OncoTargets Therapy 12, 8491–8499 (2019)PubMedCrossRef
5.
7.
Zurück zum Zitat M. Nakamoto, A.D. Bergemann, Diverse roles for the Eph family of receptor tyrosine kinases in carcinogenesis. Microsc. Res. Tech. 59(1), 58–67 (2002)PubMedCrossRef M. Nakamoto, A.D. Bergemann, Diverse roles for the Eph family of receptor tyrosine kinases in carcinogenesis. Microsc. Res. Tech. 59(1), 58–67 (2002)PubMedCrossRef
8.
Zurück zum Zitat C.W. Menges, D.J. McCance, Constitutive activation of the Raf-MAPK pathway causes negative feedback inhibition of Ras-PI3K-AKT and cellular arrest through the EphA2 receptor. Oncogene 27(20), 2934–2940 (2008)PubMedCrossRef C.W. Menges, D.J. McCance, Constitutive activation of the Raf-MAPK pathway causes negative feedback inhibition of Ras-PI3K-AKT and cellular arrest through the EphA2 receptor. Oncogene 27(20), 2934–2940 (2008)PubMedCrossRef
9.
Zurück zum Zitat H. Miao, D.Q. Li, A. Mukherjee, H. Guo, A. Petty, J. Cutter, J.P. Basilion, J. Sedor, J. Wu, D. Danielpour, A.E. Sloan, M.L. Cohen, B. Wang, EphA2 mediates ligand-dependent inhibition and ligand-independent promotion of cell migration and invasion via a reciprocal regulatory loop with Akt. Cancer Cell 16(1), 9–20 (2009)PubMedPubMedCentralCrossRef H. Miao, D.Q. Li, A. Mukherjee, H. Guo, A. Petty, J. Cutter, J.P. Basilion, J. Sedor, J. Wu, D. Danielpour, A.E. Sloan, M.L. Cohen, B. Wang, EphA2 mediates ligand-dependent inhibition and ligand-independent promotion of cell migration and invasion via a reciprocal regulatory loop with Akt. Cancer Cell 16(1), 9–20 (2009)PubMedPubMedCentralCrossRef
10.
Zurück zum Zitat A. Barquilla, E.B. Pasquale, Eph receptors and ephrins: therapeutic opportunities. Annu. Rev. Pharmacol. Toxicol. 55, 465–487 (2015)PubMedCrossRef A. Barquilla, E.B. Pasquale, Eph receptors and ephrins: therapeutic opportunities. Annu. Rev. Pharmacol. Toxicol. 55, 465–487 (2015)PubMedCrossRef
11.
Zurück zum Zitat H. Miao, E. Burnett, M. Kinch, E. Simon, B. Wang, Activation of EphA2 kinase suppresses integrin function and causes focal-adhesion-kinase dephosphorylation. Nat. Cell Biol. 2(2), 62–69 (2000)PubMedCrossRef H. Miao, E. Burnett, M. Kinch, E. Simon, B. Wang, Activation of EphA2 kinase suppresses integrin function and causes focal-adhesion-kinase dephosphorylation. Nat. Cell Biol. 2(2), 62–69 (2000)PubMedCrossRef
12.
Zurück zum Zitat Zhou Y., Yamada N., Tanaka T., Hori T., Yokoyama S., Hayakawa Y., Yano S., Fukuoka J., Koizumi K., Saiki I., Sakurai H. Crucial roles of RSK in cell motility by catalysing serine phosphorylation of EphA2. Nat. Commun. 6:7679 (2015)PubMedPubMedCentralCrossRef Zhou Y., Yamada N., Tanaka T., Hori T., Yokoyama S., Hayakawa Y., Yano S., Fukuoka J., Koizumi K., Saiki I., Sakurai H. Crucial roles of RSK in cell motility by catalysing serine phosphorylation of EphA2. Nat. Commun. 6:7679 (2015)PubMedPubMedCentralCrossRef
13.
Zurück zum Zitat H. Guo, H. Miao, L. Gerber, J. Singh, M.F. Denning, A.C. Gilliam, B. Wang, Disruption of EphA2 receptor tyrosine kinase leads to increased susceptibility to carcinogenesis in mouse skin. Cancer Res. 66(14), 7050–7058 (2006)PubMedCrossRef H. Guo, H. Miao, L. Gerber, J. Singh, M.F. Denning, A.C. Gilliam, B. Wang, Disruption of EphA2 receptor tyrosine kinase leads to increased susceptibility to carcinogenesis in mouse skin. Cancer Res. 66(14), 7050–7058 (2006)PubMedCrossRef
14.
Zurück zum Zitat B. Miao, Z. Ji, L. Tan, M. Taylor, J. Zhang, H.G. Choi, D.T. Frederick, R. Kumar, J.A. Wargo, K.T. Flaherty, N.S. Gray, H. Tsao, EPHA2 is a mediator of vemurafenib resistance and a novel therapeutic target in melanoma. Cancer Discov. 5(3), 274–287 (2015)PubMedCrossRef B. Miao, Z. Ji, L. Tan, M. Taylor, J. Zhang, H.G. Choi, D.T. Frederick, R. Kumar, J.A. Wargo, K.T. Flaherty, N.S. Gray, H. Tsao, EPHA2 is a mediator of vemurafenib resistance and a novel therapeutic target in melanoma. Cancer Discov. 5(3), 274–287 (2015)PubMedCrossRef
15.
Zurück zum Zitat G. Zhuang, D.M. Brantley-Sieders, D. Vaught, J. Yu, L. Xie, S. Wells, D. Jackson, R. Muraoka-Cook, C. Arteaga, J. Chen, Elevation of receptor tyrosine kinase EphA2 mediates resistance to trastuzumab therapy. Cancer Res. 70(1), 299–308 (2010)PubMedCrossRef G. Zhuang, D.M. Brantley-Sieders, D. Vaught, J. Yu, L. Xie, S. Wells, D. Jackson, R. Muraoka-Cook, C. Arteaga, J. Chen, Elevation of receptor tyrosine kinase EphA2 mediates resistance to trastuzumab therapy. Cancer Res. 70(1), 299–308 (2010)PubMedCrossRef
16.
Zurück zum Zitat K.R. Amato, S. Wang, L. Tan, A.K. Hastings, W. Song, C.M. Lovly, C.B. Meador, F. Ye, P. Lu, J.M. Balko, D.C. Colvin, J.M. Cates, W. Pao, N.S. Gray, J. Chen, EPHA2 Blockade Overcomes Acquired Resistance to EGFR Kinase Inhibitors in Lung Cancer. Cancer Res. 76(2), 305–318 (2016) K.R. Amato, S. Wang, L. Tan, A.K. Hastings, W. Song, C.M. Lovly, C.B. Meador, F. Ye, P. Lu, J.M. Balko, D.C. Colvin, J.M. Cates, W. Pao, N.S. Gray, J. Chen, EPHA2 Blockade Overcomes Acquired Resistance to EGFR Kinase Inhibitors in Lung Cancer. Cancer Res. 76(2), 305–318 (2016)
17.
Zurück zum Zitat D. Vaught, J. Chen, D.M. Brantley-Sieders, Regulation of mammary gland branching morphogenesis by EphA2 receptor tyrosine kinase. Mol. Biol. Cell 20(10), 2572–2581 (2009)PubMedPubMedCentralCrossRef D. Vaught, J. Chen, D.M. Brantley-Sieders, Regulation of mammary gland branching morphogenesis by EphA2 receptor tyrosine kinase. Mol. Biol. Cell 20(10), 2572–2581 (2009)PubMedPubMedCentralCrossRef
18.
Zurück zum Zitat D.P. Zelinski, N.D. Zantek, J.C. Stewart, A.R. Irizarry, M.S. Kinch, EphA2 overexpression causes tumorigenesis of mammary epithelial cells. Cancer Res. 61(5), 2301–2306 (2001)PubMed D.P. Zelinski, N.D. Zantek, J.C. Stewart, A.R. Irizarry, M.S. Kinch, EphA2 overexpression causes tumorigenesis of mammary epithelial cells. Cancer Res. 61(5), 2301–2306 (2001)PubMed
19.
Zurück zum Zitat W. Song, Y. Hwang, V.M. Youngblood, R.S. Cook, J.M. Balko, J. Chen, D.M. Brantley-Sieders, Targeting EphA2 impairs cell cycle progression and growth of basal-like/triple-negative breast cancers. Oncogene 36(40), 5620–5630 (2017)PubMedPubMedCentralCrossRef W. Song, Y. Hwang, V.M. Youngblood, R.S. Cook, J.M. Balko, J. Chen, D.M. Brantley-Sieders, Targeting EphA2 impairs cell cycle progression and growth of basal-like/triple-negative breast cancers. Oncogene 36(40), 5620–5630 (2017)PubMedPubMedCentralCrossRef
20.
Zurück zum Zitat J. Mo, B. Sun, X. Zhao, Q. Gu, X. Dong, Z. Liu, Y. Ma, N. Zhao, Y. Liu, J. Chi, R. Sun, The in-vitro spheroid culture induces a more highly differentiated but tumorigenic population from melanoma cell lines. Melanoma Res. 23(4), 254–263 (2013)PubMed J. Mo, B. Sun, X. Zhao, Q. Gu, X. Dong, Z. Liu, Y. Ma, N. Zhao, Y. Liu, J. Chi, R. Sun, The in-vitro spheroid culture induces a more highly differentiated but tumorigenic population from melanoma cell lines. Melanoma Res. 23(4), 254–263 (2013)PubMed
21.
Zurück zum Zitat L. Deng, J. Sun, X. Chen, L. Liu, D. Wu, Nek2 augments sorafenib resistance by regulating the ubiquitination and localization of beta-catenin in hepatocellular carcinoma. J. Exp. Clin. Cancer Res.: CR 38(1), 316 (2019)PubMedCrossRef L. Deng, J. Sun, X. Chen, L. Liu, D. Wu, Nek2 augments sorafenib resistance by regulating the ubiquitination and localization of beta-catenin in hepatocellular carcinoma. J. Exp. Clin. Cancer Res.: CR 38(1), 316 (2019)PubMedCrossRef
22.
Zurück zum Zitat T. Schatton, G.F. Murphy, N.Y. Frank, K. Yamaura, A.M. Waaga-Gasser, M. Gasser, Q. Zhan, S. Jordan, L.M. Duncan, C. Weishaupt, R.C. Fuhlbrigge, T.S. Kupper, M.H. Sayegh, M.H. Frank, Identification of cells initiating human melanomas. Nature 451(7176), 345–349 (2008)PubMedPubMedCentralCrossRef T. Schatton, G.F. Murphy, N.Y. Frank, K. Yamaura, A.M. Waaga-Gasser, M. Gasser, Q. Zhan, S. Jordan, L.M. Duncan, C. Weishaupt, R.C. Fuhlbrigge, T.S. Kupper, M.H. Sayegh, M.H. Frank, Identification of cells initiating human melanomas. Nature 451(7176), 345–349 (2008)PubMedPubMedCentralCrossRef
23.
Zurück zum Zitat L. Li, J. Chen, J. Wang, D. Cai, Prevalence and risk factors of diabetic peripheral neuropathy in Type 2 diabetes mellitus patients with overweight/obese in Guangdong province, China. Primary care diabetes 9(3), 191–195 (2015) L. Li, J. Chen, J. Wang, D. Cai, Prevalence and risk factors of diabetic peripheral neuropathy in Type 2 diabetes mellitus patients with overweight/obese in Guangdong province, China. Primary care diabetes 9(3), 191–195 (2015)
24.
Zurück zum Zitat A. Kassambara, C. Gourzones-Dmitriev, S. Sahota, T. Reme, J. Moreaux, H. Goldschmidt, A. Constantinou, P. Pasero, D. Hose, B. Klein, A DNA repair pathway score predicts survival in human multiple myeloma: the potential for therapeutic strategy. Oncotarget 5(9), 2487–2498 (2014)PubMedPubMedCentralCrossRef A. Kassambara, C. Gourzones-Dmitriev, S. Sahota, T. Reme, J. Moreaux, H. Goldschmidt, A. Constantinou, P. Pasero, D. Hose, B. Klein, A DNA repair pathway score predicts survival in human multiple myeloma: the potential for therapeutic strategy. Oncotarget 5(9), 2487–2498 (2014)PubMedPubMedCentralCrossRef
25.
Zurück zum Zitat M. Macrae, R.M. Neve, P. Rodriguez-Viciana, C. Haqq, J. Yeh, C.R. Chen, J.W. Gray, F. McCormick, A conditional feedback loop regulates Ras activity through EphA2. Cancer Cell 8(2), 111–118 (2005)PubMedCrossRef M. Macrae, R.M. Neve, P. Rodriguez-Viciana, C. Haqq, J. Yeh, C.R. Chen, J.W. Gray, F. McCormick, A conditional feedback loop regulates Ras activity through EphA2. Cancer Cell 8(2), 111–118 (2005)PubMedCrossRef
26.
Zurück zum Zitat O. Straume, L.A. Akslen, Importance of vascular phenotype by basic fibroblast growth factor, and influence of the angiogenic factors basic fibroblast growth factor/fibroblast growth factor receptor-1 and ephrin-A1/EphA2 on melanoma progression. Am. J. Pathol. 160(3), 1009–1019 (2002)PubMedPubMedCentralCrossRef O. Straume, L.A. Akslen, Importance of vascular phenotype by basic fibroblast growth factor, and influence of the angiogenic factors basic fibroblast growth factor/fibroblast growth factor receptor-1 and ephrin-A1/EphA2 on melanoma progression. Am. J. Pathol. 160(3), 1009–1019 (2002)PubMedPubMedCentralCrossRef
27.
Zurück zum Zitat E. Wiedemann, S. Jellinghaus, G. Ende, A. Augstein, R. Sczech, B. Wielockx, S. Weinert, R.H. Strasser, D.M. Poitz, Regulation of endothelial migration and proliferation by ephrin-A1. Cell. Signal 29, 84–95 (2017) E. Wiedemann, S. Jellinghaus, G. Ende, A. Augstein, R. Sczech, B. Wielockx, S. Weinert, R.H. Strasser, D.M. Poitz, Regulation of endothelial migration and proliferation by ephrin-A1. Cell. Signal 29, 84–95 (2017)
28.
Zurück zum Zitat X. Li, L. Wang, J.W. Gu, B. Li, W.P. Liu, Y.G. Wang, X. Zhang, H.N. Zhen, Z. Fei, Up-regulation of EphA2 and down-regulation of EphrinA1 are associated with the aggressive phenotype and poor prognosis of malignant glioma. Tumour biology: the journal of the International Society for Oncodevelopmental Biology and Medicine 31(5), 477–488 (2010) X. Li, L. Wang, J.W. Gu, B. Li, W.P. Liu, Y.G. Wang, X. Zhang, H.N. Zhen, Z. Fei, Up-regulation of EphA2 and down-regulation of EphrinA1 are associated with the aggressive phenotype and poor prognosis of malignant glioma. Tumour biology: the journal of the International Society for Oncodevelopmental Biology and Medicine 31(5), 477–488 (2010)
29.
Zurück zum Zitat J. Wykosky, W. Debinski, The EphA2 receptor and ephrinA1 ligand in solid tumors: function and therapeutic targeting. Mol. Cancer Res.: MCR 6(12), 1795–1806 (2008)PubMedCrossRef J. Wykosky, W. Debinski, The EphA2 receptor and ephrinA1 ligand in solid tumors: function and therapeutic targeting. Mol. Cancer Res.: MCR 6(12), 1795–1806 (2008)PubMedCrossRef
30.
Zurück zum Zitat K.H. Paraiso, M. Das Thakur, B. Fang, J.M. Koomen, I.V. Fedorenko, J.K. John, H. Tsao, K.T. Flaherty, V.K. Sondak, J.L. Messina, E.B. Pasquale, A. Villagra, U.N. Rao, J.M. Kirkwood, F. Meier, S. Sloot, G.T. Gibney, D. Stuart, H. Tawbi, K.S. Smalley, Ligand-independent EPHA2 signaling drives the adoption of a targeted therapy-mediated metastatic melanoma phenotype. Cancer Discov. 5(3), 264–273 (2015)PubMedCrossRef K.H. Paraiso, M. Das Thakur, B. Fang, J.M. Koomen, I.V. Fedorenko, J.K. John, H. Tsao, K.T. Flaherty, V.K. Sondak, J.L. Messina, E.B. Pasquale, A. Villagra, U.N. Rao, J.M. Kirkwood, F. Meier, S. Sloot, G.T. Gibney, D. Stuart, H. Tawbi, K.S. Smalley, Ligand-independent EPHA2 signaling drives the adoption of a targeted therapy-mediated metastatic melanoma phenotype. Cancer Discov. 5(3), 264–273 (2015)PubMedCrossRef
31.
Zurück zum Zitat W.B. Fang, D.M. Brantley-Sieders, M.A. Parker, A.D. Reith, J. Chen, A kinase-dependent role for EphA2 receptor in promoting tumor growth and metastasis. Oncogene 24(53), 7859–7868 (2005)PubMedCrossRef W.B. Fang, D.M. Brantley-Sieders, M.A. Parker, A.D. Reith, J. Chen, A kinase-dependent role for EphA2 receptor in promoting tumor growth and metastasis. Oncogene 24(53), 7859–7868 (2005)PubMedCrossRef
32.
Zurück zum Zitat K.R. Amato, S. Wang, A.K. Hastings, V.M. Youngblood, P.R. Santapuram, H. Chen, J.M. Cates, D.C. Colvin, F. Ye, D.M. Brantley-Sieders, R.S. Cook, L. Tan, N.S. Gray, J. Chen, Genetic and pharmacologic inhibition of EPHA2 promotes apoptosis in NSCLC. J. Clin. Invest. 124(5), 2037–2049; (2014) K.R. Amato, S. Wang, A.K. Hastings, V.M. Youngblood, P.R. Santapuram, H. Chen, J.M. Cates, D.C. Colvin, F. Ye, D.M. Brantley-Sieders, R.S. Cook, L. Tan, N.S. Gray, J. Chen, Genetic and pharmacologic inhibition of EPHA2 promotes apoptosis in NSCLC. J. Clin. Invest. 124(5), 2037–2049; (2014)
33.
Zurück zum Zitat Y. Sheng, J. Wei, Y. Zhang, X. Gao, Z. Wang, J. Yang, S. Yan, Y. Zhu, Z. Zhang, D. Xu, C. Wang, Y. Zheng, Q. Dong, L. Qin, Mutated EPHA2 is a target for combating lymphatic metastasis in intrahepatic cholangiocarcinoma. Int. J. Cancer 144(10), 2440–2452 (2019) Y. Sheng, J. Wei, Y. Zhang, X. Gao, Z. Wang, J. Yang, S. Yan, Y. Zhu, Z. Zhang, D. Xu, C. Wang, Y. Zheng, Q. Dong, L. Qin, Mutated EPHA2 is a target for combating lymphatic metastasis in intrahepatic cholangiocarcinoma. Int. J. Cancer 144(10), 2440–2452 (2019)
34.
Zurück zum Zitat D. Kiewlich, J. Zhang, C. Gross, W. Xia, B. Larsen, R.R. Cobb, S. Biroc, J.M. Gu, T. Sato, D.R. Light, T. Heitner, J. Willuda, D. Vogel, F. Monteclaro, A. Citkowicz, S.R. Roffler, D.A. Zajchowski, Anti-EphA2 antibodies decrease EphA2 protein levels in murine CT26 colorectal and human MDA-231 breast tumors but do not inhibit tumor growth. Neoplasia 8(1), 18–30 (2006)PubMedPubMedCentralCrossRef D. Kiewlich, J. Zhang, C. Gross, W. Xia, B. Larsen, R.R. Cobb, S. Biroc, J.M. Gu, T. Sato, D.R. Light, T. Heitner, J. Willuda, D. Vogel, F. Monteclaro, A. Citkowicz, S.R. Roffler, D.A. Zajchowski, Anti-EphA2 antibodies decrease EphA2 protein levels in murine CT26 colorectal and human MDA-231 breast tumors but do not inhibit tumor growth. Neoplasia 8(1), 18–30 (2006)PubMedPubMedCentralCrossRef
35.
Zurück zum Zitat M. Ishikawa, R. Miyahara, M. Sonobe, M. Horiuchi, T. Mennju, E. Nakayama, M. Kobayashi, R. Kikuchi, J. Kitamura, N. Imamura, C.L. Huang, H. Date, Higher expression of EphA2 and ephrin-A1 is related to favorable clinicopathological features in pathological stage I non-small cell lung carcinoma. Lung cancer 76(3), 431–438 (2012) M. Ishikawa, R. Miyahara, M. Sonobe, M. Horiuchi, T. Mennju, E. Nakayama, M. Kobayashi, R. Kikuchi, J. Kitamura, N. Imamura, C.L. Huang, H. Date, Higher expression of EphA2 and ephrin-A1 is related to favorable clinicopathological features in pathological stage I non-small cell lung carcinoma. Lung cancer 76(3), 431–438 (2012)
36.
Zurück zum Zitat M. Locard-Paulet, L. Lim, G. Veluscek, K. McMahon, J. Sinclair, A. van Weverwijk, J.D. Worboys, Y. Yuan, C.M. Isacke, C. Jorgensen, Phosphoproteomic analysis of interacting tumor and endothelial cells identifies regulatory mechanisms of transendothelial migration. Sci. Signal. 9(414), ra15 (2016)PubMedPubMedCentralCrossRef M. Locard-Paulet, L. Lim, G. Veluscek, K. McMahon, J. Sinclair, A. van Weverwijk, J.D. Worboys, Y. Yuan, C.M. Isacke, C. Jorgensen, Phosphoproteomic analysis of interacting tumor and endothelial cells identifies regulatory mechanisms of transendothelial migration. Sci. Signal. 9(414), ra15 (2016)PubMedPubMedCentralCrossRef
37.
Zurück zum Zitat T. Tawadros, M.D. Brown, C.A. Hart, N.W. Clarke, Ligand-independent activation of EphA2 by arachidonic acid induces metastasis-like behaviour in prostate cancer cells. Brit. J. Cancer 107(10), 1737–1744 (2012) T. Tawadros, M.D. Brown, C.A. Hart, N.W. Clarke, Ligand-independent activation of EphA2 by arachidonic acid induces metastasis-like behaviour in prostate cancer cells. Brit. J. Cancer 107(10), 1737–1744 (2012)
38.
Zurück zum Zitat U. Gopal, J.E. Bohonowych, C. Lema-Tome, A. Liu, E. Garrett-Mayer, B. Wang, J.S. Isaacs, A novel extracellular Hsp90 mediated co-receptor function for LRP1 regulates EphA2 dependent glioblastoma cell invasion. PloS one 6(3), e17649 (2011) U. Gopal, J.E. Bohonowych, C. Lema-Tome, A. Liu, E. Garrett-Mayer, B. Wang, J.S. Isaacs, A novel extracellular Hsp90 mediated co-receptor function for LRP1 regulates EphA2 dependent glioblastoma cell invasion. PloS one 6(3), e17649 (2011)
39.
Zurück zum Zitat R. Leveque, C. Corbet, L. Aubert, M. Guilbert, C. Lagadec, E. Adriaenssens, J. Duval, P. Finetti, D. Birnbaum, N. Magne, V. Chopin, F. Bertucci, X. Le Bourhis, R.A. Toillon, ProNGF increases breast tumor aggressiveness through functional association of TrkA with EphA2. Cancer Lett. 449, 196–206 (2019)PubMedCrossRef R. Leveque, C. Corbet, L. Aubert, M. Guilbert, C. Lagadec, E. Adriaenssens, J. Duval, P. Finetti, D. Birnbaum, N. Magne, V. Chopin, F. Bertucci, X. Le Bourhis, R.A. Toillon, ProNGF increases breast tumor aggressiveness through functional association of TrkA with EphA2. Cancer Lett. 449, 196–206 (2019)PubMedCrossRef
40.
Zurück zum Zitat M. De Robertis, L. Loiacono, C. Fusilli, M.L. Poeta, T. Mazza, M. Sanchez, L. Marchionni, E. Signori, G. Lamorte, A.L. Vescovi, J. Garcia-Foncillas, V.M. Fazio, Dysregulation of EGFR Pathway in EphA2 Cell Subpopulation Significantly Associates with Poor Prognosis in Colorectal Cancer. Clin Cancer Res 23(1), 159–170 (2017)PubMedCrossRef M. De Robertis, L. Loiacono, C. Fusilli, M.L. Poeta, T. Mazza, M. Sanchez, L. Marchionni, E. Signori, G. Lamorte, A.L. Vescovi, J. Garcia-Foncillas, V.M. Fazio, Dysregulation of EGFR Pathway in EphA2 Cell Subpopulation Significantly Associates with Poor Prognosis in Colorectal Cancer. Clin Cancer Res 23(1), 159–170 (2017)PubMedCrossRef
41.
Zurück zum Zitat M. Tandon, S.V. Vemula, S.K. Mittal, Emerging strategies for EphA2 receptor targeting for cancer therapeutics. Expert Opin. Ther. Targets 15(1), 31–51 (2011) M. Tandon, S.V. Vemula, S.K. Mittal, Emerging strategies for EphA2 receptor targeting for cancer therapeutics. Expert Opin. Ther. Targets 15(1), 31–51 (2011)
42.
Zurück zum Zitat H.M. Kluger, A.Z. Dudek, C. McCann, J. Ritacco, N. Southard, L.B. Jilaveanu, A. Molinaro, M. Sznol, A phase 2 trial of dasatinib in advanced melanoma. Cancer 117(10), 2202–2208 (2011)PubMedCrossRef H.M. Kluger, A.Z. Dudek, C. McCann, J. Ritacco, N. Southard, L.B. Jilaveanu, A. Molinaro, M. Sznol, A phase 2 trial of dasatinib in advanced melanoma. Cancer 117(10), 2202–2208 (2011)PubMedCrossRef
43.
Zurück zum Zitat Y. Kaibori, Y. Saito, Y. Nakayama, EphA2 phosphorylation at Ser897 by the Cdk1/MEK/ERK/RSK pathway regulates M-phase progression via maintenance of cortical rigidity. FASEB journal: official publication of the Federation of American Societies for Experimental Biology 33(4), 5334–5349 (2019) Y. Kaibori, Y. Saito, Y. Nakayama, EphA2 phosphorylation at Ser897 by the Cdk1/MEK/ERK/RSK pathway regulates M-phase progression via maintenance of cortical rigidity. FASEB journal: official publication of the Federation of American Societies for Experimental Biology 33(4), 5334–5349 (2019)
Metadaten
Titel
Effect of EphA2 knockdown on melanoma metastasis depends on intrinsic ephrinA1 level
verfasst von
Jing Mo
Xiulan Zhao
Xueyi Dong
Tieju Liu
Nan Zhao
Danfang Zhang
Wei Wang
Yanhui Zhang
Baocun Sun
Publikationsdatum
14.04.2020
Verlag
Springer Netherlands
Erschienen in
Cellular Oncology / Ausgabe 4/2020
Print ISSN: 2211-3428
Elektronische ISSN: 2211-3436
DOI
https://doi.org/10.1007/s13402-020-00511-x

Weitere Artikel der Ausgabe 4/2020

Cellular Oncology 4/2020 Zur Ausgabe

Neu im Fachgebiet Pathologie

Molekularpathologische Untersuchungen im Wandel der Zeit

Open Access Biomarker Leitthema

Um auch an kleinen Gewebeproben zuverlässige und reproduzierbare Ergebnisse zu gewährleisten ist eine strenge Qualitätskontrolle in jedem Schritt des Arbeitsablaufs erforderlich. Eine nicht ordnungsgemäße Prüfung oder Behandlung des …

Vergleichende Pathologie in der onkologischen Forschung

Pathologie Leitthema

Die vergleichende experimentelle Pathologie („comparative experimental pathology“) ist ein Fachbereich an der Schnittstelle von Human- und Veterinärmedizin. Sie widmet sich der vergleichenden Erforschung von Gemeinsamkeiten und Unterschieden von …

Gastrointestinale Stromatumoren

Open Access GIST CME-Artikel

Gastrointestinale Stromatumoren (GIST) stellen seit über 20 Jahren ein Paradigma für die zielgerichtete Therapie mit Tyrosinkinaseinhibitoren dar. Eine elementare Voraussetzung für eine mögliche neoadjuvante oder adjuvante Behandlung bei …

Personalisierte Medizin in der Onkologie

Aufgrund des erheblichen technologischen Fortschritts in der molekularen und genetischen Diagnostik sowie zunehmender Erkenntnisse über die molekulare Pathogenese von Krankheiten hat in den letzten zwei Jahrzehnten ein grundlegender …