Literature DB >> 28860121

NAD Synthesis Pathway Interference Is a Viable Therapeutic Strategy for Chondrosarcoma.

Elisabeth F P Peterse1, Brendy E W M van den Akker1, Bertine Niessen1, Jan Oosting1, Johnny Suijker1, Yvonne de Jong1, Erik H J Danen2, Anne-Marie Cleton-Jansen1, Judith V M G Bovée3.   

Abstract

Nicotinamide phosphoribosyltransferase (NAMPT) and nicotinic acid phosphoribosyltransferase (NAPRT) are rate-limiting enzymes in the NAD+ synthesis pathway. Chondrosarcoma is a malignant cartilage forming bone tumor, in which mutations altering isocitrate dehydrogenase-1 and -2 (IDH1 and IDH2) activity have been identified as potential driver mutations. Vulnerability for NAD+ depletion has been reported for IDH1/2-mutant cells. Here, the potency of NAMPT inhibitors as a treatment of chondrosarcoma was explored. Eleven chondrosarcoma cell lines were treated with NAMPT inhibitors, in which the effect on cell viability, colony formation, and 3D collagen invasion was assessed. The expression level of NAMPT and NAPRT transcripts in chondrosarcoma cells was determined by qRT-PCR. Methylation of the NAPRT promoter was evaluated using a previously published dataset of genome-wide methylation. In addition, a methylation dataset was used to determine methylation of the NAPRT promoter in 20 IDH1/2-mutated cartilage tumors. Chondrosarcoma cells showed a dose-dependent decrease in cell viability, 3D collagen invasion, and colony formation upon treatment with NAMPT inhibitors, in which nearly half of the cell lines demonstrated absolute IC50s in the low nanomolar range. Increasing IC50s correlated to increasing NAPRT expression levels and decreasing NAPRT promoter methylation. No correlation between IDH1/2 mutation status and sensitivity for NAMPT inhibitors was observed. Strikingly, higher methylation of the NAPRT promoter was observed in high-grade versus low-grade chondrosarcomas. In conclusion, this study identified NAMPT as a potential target for treatment of chondrosarcoma.Implications: Chondrosarcoma patients, especially those of high histologic grade with lower expression and hypermethylation of NAPRT, may benefit from inhibition of the NAD synthesis pathway. Mol Cancer Res; 15(12); 1714-21. ©2017 AACR. ©2017 American Association for Cancer Research.

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Year:  2017        PMID: 28860121     DOI: 10.1158/1541-7786.MCR-17-0293

Source DB:  PubMed          Journal:  Mol Cancer Res        ISSN: 1541-7786            Impact factor:   6.333


  16 in total

1.  Translocase of the outer mitochondrial membrane complex subunit 20 (TOMM20) facilitates cancer aggressiveness and therapeutic resistance in chondrosarcoma.

Authors:  Megan E Roche; Zhao Lin; Diana Whitaker-Menezes; Tingting Zhan; Karoly Szuhai; Judith V M G Bovee; John A Abraham; Wei Jiang; Ubaldo Martinez-Outschoorn; Atrayee Basu-Mallick
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2020-09-10       Impact factor: 5.187

2.  Exploration of the chondrosarcoma metabolome; the mTOR pathway as an important pro-survival pathway.

Authors:  Ruben D Addie; Yvonne de Jong; Gaia Alberti; Alwine B Kruisselbrink; Ivo Que; Hans Baelde; Judith V M G Bovée
Journal:  J Bone Oncol       Date:  2019-01-29       Impact factor: 4.072

3.  Radiotherapy resistance in chondrosarcoma cells; a possible correlation with alterations in cell cycle related genes.

Authors:  Yvonne de Jong; Martha Ingola; Inge H Briaire-de Bruijn; Alwine B Kruisselbrink; Sanne Venneker; Ieva Palubeckaite; Bram P A M Heijs; Anne-Marie Cleton-Jansen; Rick L M Haas; Judith V M G Bovée
Journal:  Clin Sarcoma Res       Date:  2019-05-28

4.  Association of Mental Health-Related Proteins DAXX, DRD3, and DISC1 With the Progression and Prognosis of Chondrosarcoma.

Authors:  Lile He; Xiangyu Shi; Ruiqi Chen; Zhengchun Wu; Zhulin Yang; Zhihong Li
Journal:  Front Mol Biosci       Date:  2019-11-26

Review 5.  Mutation-driven epigenetic alterations as a defining hallmark of central cartilaginous tumours, giant cell tumour of bone and chondroblastoma.

Authors:  Sanne Venneker; Karoly Szuhai; Pancras C W Hogendoorn; Judith V M G Bovée
Journal:  Virchows Arch       Date:  2019-11-14       Impact factor: 4.064

6.  Targeting the NAD Salvage Synthesis Pathway as a Novel Therapeutic Strategy for Osteosarcomas with Low NAPRT Expression.

Authors:  Natasja Franceschini; Jan Oosting; Maud Tamsma; Bertine Niessen; Inge Briaire-de Bruijn; Brendy van den Akker; Alwine B Kruisselbrink; Ieva Palubeckaitė; Judith V M G Bovée; Anne-Marie Cleton-Jansen
Journal:  Int J Mol Sci       Date:  2021-06-10       Impact factor: 5.923

7.  Genotype-targeted local therapy of glioma.

Authors:  Ganesh M Shankar; Ameya R Kirtane; Julie J Miller; Hormoz Mazdiyasni; Jaimie Rogner; Tammy Tai; Erik A Williams; Fumi Higuchi; Tareq A Juratli; Kensuke Tateishi; Mara V A Koerner; Shilpa S Tummala; Alexandria L Fink; Tristan Penson; Stephen P Schmidt; Gregory R Wojtkiewicz; Aymen Baig; Joshua M Francis; Mikael L Rinne; Julie M Batten; Tracy T Batchelor; Priscilla K Brastianos; William T Curry; Fred G Barker; Justin T Jordan; A John Iafrate; Andrew S Chi; Jochen K Lennerz; Matthew Meyerson; Robert Langer; Hiroaki Wakimoto; Giovanni Traverso; Daniel P Cahill
Journal:  Proc Natl Acad Sci U S A       Date:  2018-08-06       Impact factor: 12.779

Review 8.  NAD- and NADPH-Contributing Enzymes as Therapeutic Targets in Cancer: An Overview.

Authors:  Alvinsyah Adhityo Pramono; Gulam M Rather; Herry Herman; Keri Lestari; Joseph R Bertino
Journal:  Biomolecules       Date:  2020-02-26

Review 9.  Biological Heterogeneity of Chondrosarcoma: From (Epi) Genetics through Stemness and Deregulated Signaling to Immunophenotype.

Authors:  Agnieszka Zając; Sylwia K Król; Piotr Rutkowski; Anna M Czarnecka
Journal:  Cancers (Basel)       Date:  2021-03-15       Impact factor: 6.639

Review 10.  NAD+ metabolism, stemness, the immune response, and cancer.

Authors:  Lola E Navas; Amancio Carnero
Journal:  Signal Transduct Target Ther       Date:  2021-01-01
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