Literature DB >> 24269351

Proteome analysis of the effects of all-trans retinoic acid on human germ cell tumor cell lines.

Friedemann Honecker1, Tina Rohlfing2, Sönke Harder3, Melanie Braig2, Ad J M Gillis4, Stephanie Glaesener5, Christine Barett2, Carsten Bokemeyer2, Friedrich Buck3, Tim H Brümmendorf6, Leendert H J Looijenga4, Stefan Balabanov7.   

Abstract

We analysed the effects of all-trans retinoic acid (ATRA) on proliferation and changes in the global proteome of the nullipotent human embryonal carcinoma cell line 2102Ep and the pluripotent cell line NTERA2 cl.D1 (NT2). Differentially expressed proteins were assessed by 2D-PAGE and mass spectrometry, followed by verification and analysis of protein modifications of proteins of the retinoid pathway. We established a proteome map of the germ cell tumor (GCT) cell line NT2 showing neuronal differentiation under ATRA treatment for 7days. Using bioinformatic analyses, we identified functional groups of altered proteins and potentially involved pathways, of which changes to the organization of the cytoskeleton and anti-apoptotic effects were the most prominent. Changes observed in the expression of factors involved in the retinoid pathway under ATRA, namely an upregulation of CRBP and CRABP2, were also reflected in GCT tissues of different histologies, providing further insight into factors involved in the differentiation of these pluripotent tumors. BIOLOGICAL SIGNIFICANCE: Treatment of NT2 germ cell tumor cells with all-trans retinoic acid (ATRA) is a model to investigate differentiation. We analysed differentially expressed proteins by 2D-PAGE and mass spectrometry and provide a proteome map of NT2 cells under 7days of ATRA. By bioinformatic analyses, functional groups of proteins and involved pathways like changes to the cytoskeleton and anti-apoptotic effects were identified. Factors involved in the retinoid pathway, in particular upregulation of CRBP, CRABP1 and CRABP2, also showed differential expression in tumors with different histological subtypes, which provides insight into gene regulation under induced and spontaneous differentiation in germ cell tumors.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  CRABP; Germ cell tumor; Proteomics; Retinoic acid

Mesh:

Substances:

Year:  2013        PMID: 24269351     DOI: 10.1016/j.jprot.2013.11.010

Source DB:  PubMed          Journal:  J Proteomics        ISSN: 1874-3919            Impact factor:   4.044


  7 in total

Review 1.  Overcoming Chemotherapy Resistance in Germ Cell Tumors.

Authors:  Zuzana Országhová; Katarina Kalavska; Michal Mego; Michal Chovanec
Journal:  Biomedicines       Date:  2022-04-22

2.  Cabazitaxel overcomes cisplatin resistance in germ cell tumour cells.

Authors:  Mirjam Gerwing; Christine Jacobsen; Sergey Dyshlovoy; Jessica Hauschild; Tina Rohlfing; Christoph Oing; Simone Venz; Jan Oldenburg; Karin Oechsle; Carsten Bokemeyer; Gunhild von Amsberg; Friedemann Honecker
Journal:  J Cancer Res Clin Oncol       Date:  2016-07-16       Impact factor: 4.553

Review 3.  Molecular Mechanisms of Cisplatin Chemoresistance and Its Circumventing in Testicular Germ Cell Tumors.

Authors:  Silvia Schmidtova; Katarina Kalavska; Lucia Kucerova
Journal:  Curr Oncol Rep       Date:  2018-09-26       Impact factor: 5.075

4.  MEK inhibitors enhance therapeutic response towards ATRA in NF1 associated malignant peripheral nerve sheath tumors (MPNST) in-vitro.

Authors:  Susan Fischer-Huchzermeyer; Anna Dombrowski; Gordon Wilke; Verena Stahn; Anna Streubel; Victor Felix Mautner; Anja Harder
Journal:  PLoS One       Date:  2017-11-13       Impact factor: 3.240

Review 5.  FSH regulates RA signaling to commit spermatogonia into differentiation pathway and meiosis.

Authors:  Maryam Khanehzad; Roya Abbaszadeh; Marzieh Holakuyee; Mohammad Hossein Modarressi; Seyed Mehdi Nourashrafeddin
Journal:  Reprod Biol Endocrinol       Date:  2021-01-07       Impact factor: 5.211

6.  Targeting Germ Cell Tumors with the Newly Synthesized Flavanone-Derived Compound MLo1302 Efficiently Reduces Tumor Cell Viability and Induces Apoptosis and Cell Cycle Arrest.

Authors:  João Lobo; Ana Rita Cardoso; Vera Miranda-Gonçalves; Leendert H J Looijenga; Marie Lopez; Paola B Arimondo; Rui Henrique; Carmen Jerónimo
Journal:  Pharmaceutics       Date:  2021-01-07       Impact factor: 6.321

7.  BMP Inhibition in Seminomas Initiates Acquisition of Pluripotency via NODAL Signaling Resulting in Reprogramming to an Embryonal Carcinoma.

Authors:  Daniel Nettersheim; Sina Jostes; Rakesh Sharma; Simon Schneider; Andrea Hofmann; Humberto J Ferreira; Per Hoffmann; Glen Kristiansen; Manel B Esteller; Hubert Schorle
Journal:  PLoS Genet       Date:  2015-07-30       Impact factor: 5.917

  7 in total

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