Skip to main content
Top
Published in: Cellular Oncology 4/2018

01-08-2018 | Report

AAA+ ATPases Reptin and Pontin as potential diagnostic and prognostic biomarkers in salivary gland cancer - a short report

Authors: Jan-Henrik Mikesch, Wolfgang Hartmann, Linus Angenendt, Otmar Huber, Christoph Schliemann, Maria Francisca Arteaga, Eva Wardelmann, Claudia Rudack, Wolfgang E. Berdel, Markus Stenner, Inga Grünewald

Published in: Cellular Oncology | Issue 4/2018

Login to get access

Abstract

Purpose

Salivary gland cancer (SGC) is a rare and heterogeneous disease with significant differences in recurrence and metastasis characteristics. As yet, little is known about the mechanisms underlying the initiation and/or progression of these diverse tumors. In recent years, the AAA+ ATPase family members Pontin (RuvBL1, Tip49a) and Reptin (RuvBL2, Tip49b) have been implicated in various processes, including transcription regulation, chromatin remodeling and DNA damage repair, that are frequently deregulated in cancer. The aim of this study was to assess the clinical and functional significance of Reptin and Pontin expression in SGC.

Methods

Immunohistochemical staining of Pontin, Reptin, β-catenin, Cyclin D1, TP53 and MIB-1 was performed on a collection of 94 SGC tumor samples comprising 13 different histological subtypes using tissue microarrays.

Results

We found that Reptin and Pontin were expressed in the majority of SGC samples across all histological subtypes. Patients with a high Reptin expression showed a significantly inferior 5-year overall survival rate compared to patients with a low Reptin expression (47.7% versus 78.3%; p = 0.033), whereas no such difference was observed for Pontin. A high Reptin expression strongly correlated with a high expression of the proliferation marker MIB-1 (p = 0.003), the cell cycle regulator Cyclin D1 (p = 0.006), accumulation of TP53 as a surrogate p53 mutation marker (p = 0.042) and cytoplasmic β-catenin expression (p = 0.002). Increased Pontin expression was found to significantly correlate with both cytoplasmic and nuclear β-catenin expression (p = 0.037 and p = 0.018, respectively), which is indicative for its oncogenic function.

Conclusions

Our results suggest a role of Reptin and Pontin in SGC tumor progression and/or patient survival. Therefore, SGC patients exhibiting a high Reptin expression may benefit from more aggressive therapeutic regimens. Future studies should clarify whether such patients may be considered for more radical surgery, extended adjuvant therapy and/or targeted therapy.
Literature
8.
go back to reference J.G. Armstrong, L.B. Harrison, R.H. Spiro, D.E. Fass, E.W. Strong, Z.Y. Fuks, Malignant tumors of major salivary gland origin. A matched-pair analysis of the role of combined surgery and postoperative radiotherapy. Arch Otolaryngol Head Neck Surg 116, 290–293 (1990)CrossRefPubMed J.G. Armstrong, L.B. Harrison, R.H. Spiro, D.E. Fass, E.W. Strong, Z.Y. Fuks, Malignant tumors of major salivary gland origin. A matched-pair analysis of the role of combined surgery and postoperative radiotherapy. Arch Otolaryngol Head Neck Surg 116, 290–293 (1990)CrossRefPubMed
10.
go back to reference E.S. Choi, S. Oh, B. Jang, H.J. Yu, J.A. Shin, N.P. Cho, I.H. Yang, D.H. Won, H.J. Kwon, S.D. Hong, S.D. Cho, Silymarin and its active component silibinin act as novel therapeutic alternatives for salivary gland cancer by targeting the ERK1/2-Bim signaling cascade. Cell Oncol 40, 235–246 (2017). https://doi.org/10.1007/s13402-017-0318-8 CrossRef E.S. Choi, S. Oh, B. Jang, H.J. Yu, J.A. Shin, N.P. Cho, I.H. Yang, D.H. Won, H.J. Kwon, S.D. Hong, S.D. Cho, Silymarin and its active component silibinin act as novel therapeutic alternatives for salivary gland cancer by targeting the ERK1/2-Bim signaling cascade. Cell Oncol 40, 235–246 (2017). https://​doi.​org/​10.​1007/​s13402-017-0318-8 CrossRef
20.
go back to reference V. Haurie, L. Menard, A. Nicou, C. Touriol, P. Metzler, J. Fernandez, D. Taras, P. Lestienne, C. Balabaud, P. Bioulac-Sage, H. Prats, J. Zucman-Rossi, J. Rosenbaum, Adenosine triphosphatase pontin is overexpressed in hepatocellular carcinoma and coregulated with reptin through a new posttranslational mechanism. Hepatology 50, 1871–1883 (2009). https://doi.org/10.1002/hep.23215 CrossRefPubMedPubMedCentral V. Haurie, L. Menard, A. Nicou, C. Touriol, P. Metzler, J. Fernandez, D. Taras, P. Lestienne, C. Balabaud, P. Bioulac-Sage, H. Prats, J. Zucman-Rossi, J. Rosenbaum, Adenosine triphosphatase pontin is overexpressed in hepatocellular carcinoma and coregulated with reptin through a new posttranslational mechanism. Hepatology 50, 1871–1883 (2009). https://​doi.​org/​10.​1002/​hep.​23215 CrossRefPubMedPubMedCentral
22.
23.
go back to reference A. Bauer, O. Huber, R. Kemler, Pontin52, an interaction partner of beta-catenin, binds to the TATA box binding protein. Proc Natl Acad Sci U S A 95, 14787–14792 (1998)CrossRefPubMedPubMedCentral A. Bauer, O. Huber, R. Kemler, Pontin52, an interaction partner of beta-catenin, binds to the TATA box binding protein. Proc Natl Acad Sci U S A 95, 14787–14792 (1998)CrossRefPubMedPubMedCentral
26.
go back to reference A. Skalova, T. Vanecek, R. Sima, J. Laco, I. Weinreb, B. Perez-Ordonez, I. Starek, M. Geierova, R.H. Simpson, F. Passador-Santos, A. Ryska, I. Leivo, Z. Kinkor, M. Michal, Mammary analogue secretory carcinoma of salivary glands, containing the ETV6-NTRK3 fusion gene: A hitherto undescribed salivary gland tumor entity. Am J Surg Pathol 34, 599–608 (2010). https://doi.org/10.1097/PAS.0b013e3181d9efcc PubMedCrossRef A. Skalova, T. Vanecek, R. Sima, J. Laco, I. Weinreb, B. Perez-Ordonez, I. Starek, M. Geierova, R.H. Simpson, F. Passador-Santos, A. Ryska, I. Leivo, Z. Kinkor, M. Michal, Mammary analogue secretory carcinoma of salivary glands, containing the ETV6-NTRK3 fusion gene: A hitherto undescribed salivary gland tumor entity. Am J Surg Pathol 34, 599–608 (2010). https://​doi.​org/​10.​1097/​PAS.​0b013e3181d9efcc​ PubMedCrossRef
27.
go back to reference N. Friedrichs, L. Kriegl, C. Poremba, K.L. Schaefer, H.E. Gabbert, A. Shimomura, E. Paggen, S. Merkelbach-Bruse, R. Buettner, Pitfalls in the detection of t(11;22) translocation by fluorescence in situ hybridization and RT-PCR: A single-blinded study. Diagn Mol Pathol 15, 83–89 (2006)CrossRefPubMed N. Friedrichs, L. Kriegl, C. Poremba, K.L. Schaefer, H.E. Gabbert, A. Shimomura, E. Paggen, S. Merkelbach-Bruse, R. Buettner, Pitfalls in the detection of t(11;22) translocation by fluorescence in situ hybridization and RT-PCR: A single-blinded study. Diagn Mol Pathol 15, 83–89 (2006)CrossRefPubMed
28.
go back to reference H.U. Schildhaus, L.C. Heukamp, S. Merkelbach-Bruse, K. Riesner, K. Schmitz, E. Binot, E. Paggen, K. Albus, W. Schulte, Y.D. Ko, A. Schlesinger, S. Ansen, W. Engel-Riedel, M. Brockmann, M. Serke, U. Gerigk, S. Huss, F. Goke, S. Perner, K. Hekmat, K.F. Frank, M. Reiser, R. Schnell, M. Bos, C. Mattonet, M. Sos, E. Stoelben, J. Wolf, T. Zander, R. Buettner, Definition of a fluorescence in-situ hybridization score identifies high- and low-level FGFR1 amplification types in squamous cell lung cancer. Mod Pathol 25, 1473–1480 (2012). https://doi.org/10.1038/modpathol.2012.102 CrossRefPubMedPubMedCentral H.U. Schildhaus, L.C. Heukamp, S. Merkelbach-Bruse, K. Riesner, K. Schmitz, E. Binot, E. Paggen, K. Albus, W. Schulte, Y.D. Ko, A. Schlesinger, S. Ansen, W. Engel-Riedel, M. Brockmann, M. Serke, U. Gerigk, S. Huss, F. Goke, S. Perner, K. Hekmat, K.F. Frank, M. Reiser, R. Schnell, M. Bos, C. Mattonet, M. Sos, E. Stoelben, J. Wolf, T. Zander, R. Buettner, Definition of a fluorescence in-situ hybridization score identifies high- and low-level FGFR1 amplification types in squamous cell lung cancer. Mod Pathol 25, 1473–1480 (2012). https://​doi.​org/​10.​1038/​modpathol.​2012.​102 CrossRefPubMedPubMedCentral
30.
33.
go back to reference M.V. Suzzi, A. Alessi, C. Bertarelli, A. Cancellieri, L. Procaccio, D. Dall'olio, P. Laudadio, Prognostic relevance of cell proliferation in major salivary gland carcinomas. Acta Otorhinolaryngol Ital 25, 161–168 (2005)PubMed M.V. Suzzi, A. Alessi, C. Bertarelli, A. Cancellieri, L. Procaccio, D. Dall'olio, P. Laudadio, Prognostic relevance of cell proliferation in major salivary gland carcinomas. Acta Otorhinolaryngol Ital 25, 161–168 (2005)PubMed
34.
go back to reference C.J. Gottardi, E. Wong, B.M. Gumbiner, E-cadherin suppresses cellular transformation by inhibiting beta-catenin signaling in an adhesion-independent manner. J Cell Biol 153, 1049–1060 (2001)CrossRefPubMedPubMedCentral C.J. Gottardi, E. Wong, B.M. Gumbiner, E-cadherin suppresses cellular transformation by inhibiting beta-catenin signaling in an adhesion-independent manner. J Cell Biol 153, 1049–1060 (2001)CrossRefPubMedPubMedCentral
36.
go back to reference W. Rottbauer, A.J. Saurin, H. Lickert, X. Shen, C.G. Burns, Z.G. Wo, R. Kemler, R. Kingston, C. Wu, M. Fishman, Reptin and pontin antagonistically regulate heart growth in zebrafish embryos. Cell 111, 661–672 (2002)CrossRefPubMed W. Rottbauer, A.J. Saurin, H. Lickert, X. Shen, C.G. Burns, Z.G. Wo, R. Kemler, R. Kingston, C. Wu, M. Fishman, Reptin and pontin antagonistically regulate heart growth in zebrafish embryos. Cell 111, 661–672 (2002)CrossRefPubMed
Metadata
Title
AAA+ ATPases Reptin and Pontin as potential diagnostic and prognostic biomarkers in salivary gland cancer - a short report
Authors
Jan-Henrik Mikesch
Wolfgang Hartmann
Linus Angenendt
Otmar Huber
Christoph Schliemann
Maria Francisca Arteaga
Eva Wardelmann
Claudia Rudack
Wolfgang E. Berdel
Markus Stenner
Inga Grünewald
Publication date
01-08-2018
Publisher
Springer Netherlands
Published in
Cellular Oncology / Issue 4/2018
Print ISSN: 2211-3428
Electronic ISSN: 2211-3436
DOI
https://doi.org/10.1007/s13402-018-0382-8

Other articles of this Issue 4/2018

Cellular Oncology 4/2018 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine