Literature DB >> 36214254

EphA1 receptor tyrosine kinase is localized to the nucleus in rhabdomyosarcoma from multiple species.

Ronnie LaCombe1,2, Alessandra Cecchini1,2, Morgan Seibert1, Ddw Cornelison1,2.   

Abstract

While the typical role of receptor tyrosine kinases is to receive and transmit signals at the cell surface, in some cellular contexts (particularly transformed cells) they may also act as nuclear proteins. Aberrant nuclear localization of receptor tyrosine kinases associated with transformation often enhances the transformed phenotype (i.e. nuclear ErbBs promote tumor progression in breast cancer). Rhabdomyosarcoma (RMS), the most common soft tissue tumor in children, develops to resemble immature skeletal muscle and has been proposed to derive from muscle stem/progenitor cells (satellite cells). It is an aggressive cancer with a 5-year survival rate of 33% if it has metastasized. Eph receptor tyrosine kinases have been implicated in the development and progression of many other tumor types, but there are only two published studies of Ephs localizing to the nucleus of any cell type and to date no nuclear RTKs have been identified in RMS. In a screen for protein expression of Ephs in canine RMS primary tumors as well as mouse and human RMS cell lines, we noted strong expression of EphA1 in the nucleus of interphase cells in tumors from all three species. This localization pattern changes in dividing cells, with EphA1 localizing to the nucleus or the cytoplasm depending on the phase of the cell cycle. These data represent the first case of a nuclear RTK in RMS, and the first time that EphA1 has been detected in the nucleus of any cell type.
© 2022. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Eph/ephrin; Protein localization; Rhabdomyosarcoma

Mesh:

Substances:

Year:  2022        PMID: 36214254      PMCID: PMC9581518          DOI: 10.1242/bio.059352

Source DB:  PubMed          Journal:  Biol Open        ISSN: 2046-6390            Impact factor:   2.643


  55 in total

1.  Pax7 is required for the specification of myogenic satellite cells.

Authors:  P Seale; L A Sabourin; A Girgis-Gabardo; A Mansouri; P Gruss; M A Rudnicki
Journal:  Cell       Date:  2000-09-15       Impact factor: 41.582

2.  Eph/ephrin interactions modulate muscle satellite cell motility and patterning.

Authors:  Danny A Stark; Rowan M Karvas; Ashley L Siegel; D D W Cornelison
Journal:  Development       Date:  2011-11-09       Impact factor: 6.868

Review 3.  Mechanisms of protein localization.

Authors:  T J Silhavy; S A Benson; S D Emr
Journal:  Microbiol Rev       Date:  1983-09

Review 4.  ERBB receptors and cancer: the complexity of targeted inhibitors.

Authors:  Nancy E Hynes; Heidi A Lane
Journal:  Nat Rev Cancer       Date:  2005-05       Impact factor: 60.716

5.  Sca-1 negatively regulates proliferation and differentiation of muscle cells.

Authors:  Patrick O Mitchell; Todd Mills; Roddy S O'Connor; Erik R Kline; Timothy Graubert; Elaine Dzierzak; Grace K Pavlath
Journal:  Dev Biol       Date:  2005-07-01       Impact factor: 3.582

Review 6.  The protein tyrosine kinase family of the human genome.

Authors:  D R Robinson; Y M Wu; S F Lin
Journal:  Oncogene       Date:  2000-11-20       Impact factor: 9.867

Review 7.  ErbB4/HER4: role in mammary gland development, differentiation and growth inhibition.

Authors:  Rebecca S Muraoka-Cook; Shu-Mang Feng; Karen E Strunk; H Shelton Earp
Journal:  J Mammary Gland Biol Neoplasia       Date:  2008-04-25       Impact factor: 2.673

8.  Distribution, gene expression, and functional role of EphA4 during ossification.

Authors:  Chisa Kuroda; Satoshi Kubota; Kazumi Kawata; Eriko Aoyama; Kumi Sumiyoshi; Morihiko Oka; Miho Inoue; Shogo Minagi; Masaharu Takigawa
Journal:  Biochem Biophys Res Commun       Date:  2008-07-02       Impact factor: 3.575

Review 9.  Regulation of tumor initiation and metastatic progression by Eph receptor tyrosine kinases.

Authors:  Jin Chen
Journal:  Adv Cancer Res       Date:  2012       Impact factor: 6.242

10.  Phosphorylation-induced rearrangement of the histone H3 NH2-terminal domain during mitotic chromosome condensation.

Authors:  D M Sauvé; H J Anderson; J M Ray; W M James; M Roberge
Journal:  J Cell Biol       Date:  1999-04-19       Impact factor: 10.539

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.