The Experts below are selected from a list of 189 Experts worldwide ranked by ideXlab platform
Ali G. Turhan - One of the best experts on this subject based on the ideXlab platform.
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Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2B (MEN2B) Syndrome with "highest risk" RET mutation.
Stem cell research, 2017Co-Authors: Annelise Bennaceur-griscelli, J Hadoux, O Féraud, P Opolon, D Divers, E Gobbo, M Schlumberger, F Griscelli, Ali G. TurhanAbstract:Multiple Endocrine Neoplasia Type 2B (MEN2B) is a Cancer-Predisposing Syndrome that affects patients with germline RET mutations. The clinical spectrum of the Syndrome includes medullary thyroid carcinoma (MTC) and pheochromocytoma. Currently, there is no satisfactory model recapitulating all the features of the disease especially at the level of stem cells. We generated induced pluripotent stem cells (iPSCs) from a patient with RET mutation at codon 918 who developed pheochromocytoma and MTC. These iPSC had normal karyotype, harboured the RETM918T mutation and expressed pluripotency hallmarks. A comprehensive pathological assessment of teratoma was performed after injection in immunodeficient mice.
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Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2A (MEN2A) Syndrome with RET mutation.
Stem cell research, 2016Co-Authors: Julien Hadoux, Olivier Feraud, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin Schlumberger, Annelise Bennaceur-griscelli, Ali G. TurhanAbstract:Multiple Endocrine Neoplasia Type 2B (MEN2B) is a Cancer-Predisposing Syndrome that affects patients with germline RET mutations. The clinical spectrum of the Syndrome includes medullary thyroid carcinoma (MTC) and pheochromocytoma. Currently, there is no satisfactory model recapitulating all the features of the disease especially at the level of stem cells. We generated induced pluripotent stem cells (iPSCs) from a patient with RET mutation at codon 918 who developed pheochromocytoma and MTC. These iPSC had normal karyotype, harboured the RETM918T mutation and expressed pluripotency hallmarks. A comprehensive pathological assessment of teratoma was performed after injection in immunodeficient mice.
Martin Schlumberger - One of the best experts on this subject based on the ideXlab platform.
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Transcriptional landscape of a RETC634Y-mutated iPSC and its CRISPR-corrected isogenic control reveals the putative role of EGR1 transcriptional program in the development of multiple endocrine neoplasia type 2A-associated Cancers.
Stem cell research, 2017Co-Authors: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin SchlumbergerAbstract:MEN2A is a hereditary Cancer-Predisposing Syndrome that affects patients with germline RET mutations. The effects of this oncogenic tyrosine kinase in the context of primitive stem cells are not known. In order to study these events, we generated a MEN2A induced Pluripotent Stem Cell (iPSC) line from a patient with RET mutation and an isogenic counterpart by CRISPR-Cas9 correction of the mutation. Whole exome sequencing of iPSC before and after CRISPR-Cas9 genome edition revealed no major exonic off target effect of the CRISPR correction. However, an integrative differential gene expression analysis of iPSC with oncogenic RETC634Y and its gene-corrected iPSC with RETY634C as well as RETwt iPSCs revealed activation of the Early Growth Response 1 (EGR1) transcriptional program in RET-mutated iPSC, a pathway shown to be involved in RET-induced oncogenesis. These data constitute the first proof of concept of the feasibility of the use of an iPSC and its genome-corrected counterpart to unravel the molecular mechanisms underlying the development of the hereditary MEN2A Cancer Predisposing Syndrome.
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Abstract 2483: Generation of patient-specific and genome-edited MEN2A patient-derived induced pluripotent stem cells as novel tools for drug screening
Tumor Biology, 2016Co-Authors: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin SchlumbergerAbstract:Introduction MEN2A is a Cancer-Predisposing Syndrome that affects patients with germline RET mutations. Animal models do not faithfully recapitulate the full clinical spectrum of the disease. Moreover, it has been suggested that primitive malignant stem cells could be at the origin of resistances and relapses in patients treated with standard chemotherapy. In order to modelling MEN2A malignant primitive stem cells, we have induced to pluripotency MEN2A peripheral blood mononuclear cells from patients who developed medullary thyroid carcinoma harboring “high risk” or “moderate risk” RET mutation. Methods PBMC from patients with germline RETC620R and RetC634Y mutations were reprogrammed into pluripotent stem cells using Sendai-virus mediated Oct4, Sox2, Klf4 and c-Myc gene transfer. An isogenic IPSC line was generated by genome editing, using CRISPR-Cas9 to correct the “high risk” RETC634Y mutation. Hallmarks of pluripotency, genotype and phenotypes were characterized. Results Pluripotency behaviour of each IPSC line was confirmed in vitro (EBs, and pluripotent markers) and in vivo (teratoma assay in immunodeficient mice). Genome edition of the RETC634Y iPSC led to the generation of the RETY634C isogenic control iPSC. Ret expression was confirmed on both RETC634Y and RETY634C. In order to determine the accuracy and absence of off-target effects, we have performed a whole exome sequencing of both RET-mutated and RET-corrected IPSCs. These experiments revealed some off target effects of the CRISPR-mediated gene edition. Gene-array datas revealed an increased expression of neuronal development-related set of genes in RETC634Y iPSC, as compared to RETY634C control, that may account for the development of certain MEN2A features. Treatment of IPSC with vandetanib, a Ret inhibitor, led to a decrease of iPSC colonies formation in RETC634Y mutated iPSC compared to RETY634C, suggesting that RET-iPSC could serve as a plateform drug screening model. The comprehensive pathological assessment of IPSC RET-mutated and corrected derived-teratoma did not reveal, at this point, any neuroendocrine tumor-reminiscent structure. Conclusion We report here the first MEN2A-iPSC from “high risk” RETC634Y iPSC and its genome-edited isogenic normal IPSC, with their genomic profiling by whole exome sequencing. These well caracterized RET-IPSC will allow to develop cell-based assays in high throughput screening for drug discovery and to model MEN2A. Citation Format: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin Schlumberger, Annelise Bennaceur-Griscelli, Ali Turhan. Generation of patient-specific and genome-edited MEN2A patient-derived induced pluripotent stem cells as novel tools for drug screening. [abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA. Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr 2483.
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Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2A (MEN2A) Syndrome with RET mutation.
Stem cell research, 2016Co-Authors: Julien Hadoux, Olivier Feraud, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin Schlumberger, Annelise Bennaceur-griscelli, Ali G. TurhanAbstract:Multiple Endocrine Neoplasia Type 2B (MEN2B) is a Cancer-Predisposing Syndrome that affects patients with germline RET mutations. The clinical spectrum of the Syndrome includes medullary thyroid carcinoma (MTC) and pheochromocytoma. Currently, there is no satisfactory model recapitulating all the features of the disease especially at the level of stem cells. We generated induced pluripotent stem cells (iPSCs) from a patient with RET mutation at codon 918 who developed pheochromocytoma and MTC. These iPSC had normal karyotype, harboured the RETM918T mutation and expressed pluripotency hallmarks. A comprehensive pathological assessment of teratoma was performed after injection in immunodeficient mice.
Julien Hadoux - One of the best experts on this subject based on the ideXlab platform.
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Transcriptional landscape of a RETC634Y-mutated iPSC and its CRISPR-corrected isogenic control reveals the putative role of EGR1 transcriptional program in the development of multiple endocrine neoplasia type 2A-associated Cancers.
Stem cell research, 2017Co-Authors: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin SchlumbergerAbstract:MEN2A is a hereditary Cancer-Predisposing Syndrome that affects patients with germline RET mutations. The effects of this oncogenic tyrosine kinase in the context of primitive stem cells are not known. In order to study these events, we generated a MEN2A induced Pluripotent Stem Cell (iPSC) line from a patient with RET mutation and an isogenic counterpart by CRISPR-Cas9 correction of the mutation. Whole exome sequencing of iPSC before and after CRISPR-Cas9 genome edition revealed no major exonic off target effect of the CRISPR correction. However, an integrative differential gene expression analysis of iPSC with oncogenic RETC634Y and its gene-corrected iPSC with RETY634C as well as RETwt iPSCs revealed activation of the Early Growth Response 1 (EGR1) transcriptional program in RET-mutated iPSC, a pathway shown to be involved in RET-induced oncogenesis. These data constitute the first proof of concept of the feasibility of the use of an iPSC and its genome-corrected counterpart to unravel the molecular mechanisms underlying the development of the hereditary MEN2A Cancer Predisposing Syndrome.
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Abstract 2483: Generation of patient-specific and genome-edited MEN2A patient-derived induced pluripotent stem cells as novel tools for drug screening
Tumor Biology, 2016Co-Authors: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin SchlumbergerAbstract:Introduction MEN2A is a Cancer-Predisposing Syndrome that affects patients with germline RET mutations. Animal models do not faithfully recapitulate the full clinical spectrum of the disease. Moreover, it has been suggested that primitive malignant stem cells could be at the origin of resistances and relapses in patients treated with standard chemotherapy. In order to modelling MEN2A malignant primitive stem cells, we have induced to pluripotency MEN2A peripheral blood mononuclear cells from patients who developed medullary thyroid carcinoma harboring “high risk” or “moderate risk” RET mutation. Methods PBMC from patients with germline RETC620R and RetC634Y mutations were reprogrammed into pluripotent stem cells using Sendai-virus mediated Oct4, Sox2, Klf4 and c-Myc gene transfer. An isogenic IPSC line was generated by genome editing, using CRISPR-Cas9 to correct the “high risk” RETC634Y mutation. Hallmarks of pluripotency, genotype and phenotypes were characterized. Results Pluripotency behaviour of each IPSC line was confirmed in vitro (EBs, and pluripotent markers) and in vivo (teratoma assay in immunodeficient mice). Genome edition of the RETC634Y iPSC led to the generation of the RETY634C isogenic control iPSC. Ret expression was confirmed on both RETC634Y and RETY634C. In order to determine the accuracy and absence of off-target effects, we have performed a whole exome sequencing of both RET-mutated and RET-corrected IPSCs. These experiments revealed some off target effects of the CRISPR-mediated gene edition. Gene-array datas revealed an increased expression of neuronal development-related set of genes in RETC634Y iPSC, as compared to RETY634C control, that may account for the development of certain MEN2A features. Treatment of IPSC with vandetanib, a Ret inhibitor, led to a decrease of iPSC colonies formation in RETC634Y mutated iPSC compared to RETY634C, suggesting that RET-iPSC could serve as a plateform drug screening model. The comprehensive pathological assessment of IPSC RET-mutated and corrected derived-teratoma did not reveal, at this point, any neuroendocrine tumor-reminiscent structure. Conclusion We report here the first MEN2A-iPSC from “high risk” RETC634Y iPSC and its genome-edited isogenic normal IPSC, with their genomic profiling by whole exome sequencing. These well caracterized RET-IPSC will allow to develop cell-based assays in high throughput screening for drug discovery and to model MEN2A. Citation Format: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin Schlumberger, Annelise Bennaceur-Griscelli, Ali Turhan. Generation of patient-specific and genome-edited MEN2A patient-derived induced pluripotent stem cells as novel tools for drug screening. [abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA. Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr 2483.
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Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2A (MEN2A) Syndrome with RET mutation.
Stem cell research, 2016Co-Authors: Julien Hadoux, Olivier Feraud, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin Schlumberger, Annelise Bennaceur-griscelli, Ali G. TurhanAbstract:Multiple Endocrine Neoplasia Type 2B (MEN2B) is a Cancer-Predisposing Syndrome that affects patients with germline RET mutations. The clinical spectrum of the Syndrome includes medullary thyroid carcinoma (MTC) and pheochromocytoma. Currently, there is no satisfactory model recapitulating all the features of the disease especially at the level of stem cells. We generated induced pluripotent stem cells (iPSCs) from a patient with RET mutation at codon 918 who developed pheochromocytoma and MTC. These iPSC had normal karyotype, harboured the RETM918T mutation and expressed pluripotency hallmarks. A comprehensive pathological assessment of teratoma was performed after injection in immunodeficient mice.
Olivier Feraud - One of the best experts on this subject based on the ideXlab platform.
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Transcriptional landscape of a RETC634Y-mutated iPSC and its CRISPR-corrected isogenic control reveals the putative role of EGR1 transcriptional program in the development of multiple endocrine neoplasia type 2A-associated Cancers.
Stem cell research, 2017Co-Authors: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin SchlumbergerAbstract:MEN2A is a hereditary Cancer-Predisposing Syndrome that affects patients with germline RET mutations. The effects of this oncogenic tyrosine kinase in the context of primitive stem cells are not known. In order to study these events, we generated a MEN2A induced Pluripotent Stem Cell (iPSC) line from a patient with RET mutation and an isogenic counterpart by CRISPR-Cas9 correction of the mutation. Whole exome sequencing of iPSC before and after CRISPR-Cas9 genome edition revealed no major exonic off target effect of the CRISPR correction. However, an integrative differential gene expression analysis of iPSC with oncogenic RETC634Y and its gene-corrected iPSC with RETY634C as well as RETwt iPSCs revealed activation of the Early Growth Response 1 (EGR1) transcriptional program in RET-mutated iPSC, a pathway shown to be involved in RET-induced oncogenesis. These data constitute the first proof of concept of the feasibility of the use of an iPSC and its genome-corrected counterpart to unravel the molecular mechanisms underlying the development of the hereditary MEN2A Cancer Predisposing Syndrome.
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Abstract 2483: Generation of patient-specific and genome-edited MEN2A patient-derived induced pluripotent stem cells as novel tools for drug screening
Tumor Biology, 2016Co-Authors: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin SchlumbergerAbstract:Introduction MEN2A is a Cancer-Predisposing Syndrome that affects patients with germline RET mutations. Animal models do not faithfully recapitulate the full clinical spectrum of the disease. Moreover, it has been suggested that primitive malignant stem cells could be at the origin of resistances and relapses in patients treated with standard chemotherapy. In order to modelling MEN2A malignant primitive stem cells, we have induced to pluripotency MEN2A peripheral blood mononuclear cells from patients who developed medullary thyroid carcinoma harboring “high risk” or “moderate risk” RET mutation. Methods PBMC from patients with germline RETC620R and RetC634Y mutations were reprogrammed into pluripotent stem cells using Sendai-virus mediated Oct4, Sox2, Klf4 and c-Myc gene transfer. An isogenic IPSC line was generated by genome editing, using CRISPR-Cas9 to correct the “high risk” RETC634Y mutation. Hallmarks of pluripotency, genotype and phenotypes were characterized. Results Pluripotency behaviour of each IPSC line was confirmed in vitro (EBs, and pluripotent markers) and in vivo (teratoma assay in immunodeficient mice). Genome edition of the RETC634Y iPSC led to the generation of the RETY634C isogenic control iPSC. Ret expression was confirmed on both RETC634Y and RETY634C. In order to determine the accuracy and absence of off-target effects, we have performed a whole exome sequencing of both RET-mutated and RET-corrected IPSCs. These experiments revealed some off target effects of the CRISPR-mediated gene edition. Gene-array datas revealed an increased expression of neuronal development-related set of genes in RETC634Y iPSC, as compared to RETY634C control, that may account for the development of certain MEN2A features. Treatment of IPSC with vandetanib, a Ret inhibitor, led to a decrease of iPSC colonies formation in RETC634Y mutated iPSC compared to RETY634C, suggesting that RET-iPSC could serve as a plateform drug screening model. The comprehensive pathological assessment of IPSC RET-mutated and corrected derived-teratoma did not reveal, at this point, any neuroendocrine tumor-reminiscent structure. Conclusion We report here the first MEN2A-iPSC from “high risk” RETC634Y iPSC and its genome-edited isogenic normal IPSC, with their genomic profiling by whole exome sequencing. These well caracterized RET-IPSC will allow to develop cell-based assays in high throughput screening for drug discovery and to model MEN2A. Citation Format: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin Schlumberger, Annelise Bennaceur-Griscelli, Ali Turhan. Generation of patient-specific and genome-edited MEN2A patient-derived induced pluripotent stem cells as novel tools for drug screening. [abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA. Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr 2483.
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Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2A (MEN2A) Syndrome with RET mutation.
Stem cell research, 2016Co-Authors: Julien Hadoux, Olivier Feraud, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin Schlumberger, Annelise Bennaceur-griscelli, Ali G. TurhanAbstract:Multiple Endocrine Neoplasia Type 2B (MEN2B) is a Cancer-Predisposing Syndrome that affects patients with germline RET mutations. The clinical spectrum of the Syndrome includes medullary thyroid carcinoma (MTC) and pheochromocytoma. Currently, there is no satisfactory model recapitulating all the features of the disease especially at the level of stem cells. We generated induced pluripotent stem cells (iPSCs) from a patient with RET mutation at codon 918 who developed pheochromocytoma and MTC. These iPSC had normal karyotype, harboured the RETM918T mutation and expressed pluripotency hallmarks. A comprehensive pathological assessment of teratoma was performed after injection in immunodeficient mice.
Paule Opolon - One of the best experts on this subject based on the ideXlab platform.
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Transcriptional landscape of a RETC634Y-mutated iPSC and its CRISPR-corrected isogenic control reveals the putative role of EGR1 transcriptional program in the development of multiple endocrine neoplasia type 2A-associated Cancers.
Stem cell research, 2017Co-Authors: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin SchlumbergerAbstract:MEN2A is a hereditary Cancer-Predisposing Syndrome that affects patients with germline RET mutations. The effects of this oncogenic tyrosine kinase in the context of primitive stem cells are not known. In order to study these events, we generated a MEN2A induced Pluripotent Stem Cell (iPSC) line from a patient with RET mutation and an isogenic counterpart by CRISPR-Cas9 correction of the mutation. Whole exome sequencing of iPSC before and after CRISPR-Cas9 genome edition revealed no major exonic off target effect of the CRISPR correction. However, an integrative differential gene expression analysis of iPSC with oncogenic RETC634Y and its gene-corrected iPSC with RETY634C as well as RETwt iPSCs revealed activation of the Early Growth Response 1 (EGR1) transcriptional program in RET-mutated iPSC, a pathway shown to be involved in RET-induced oncogenesis. These data constitute the first proof of concept of the feasibility of the use of an iPSC and its genome-corrected counterpart to unravel the molecular mechanisms underlying the development of the hereditary MEN2A Cancer Predisposing Syndrome.
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Abstract 2483: Generation of patient-specific and genome-edited MEN2A patient-derived induced pluripotent stem cells as novel tools for drug screening
Tumor Biology, 2016Co-Authors: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin SchlumbergerAbstract:Introduction MEN2A is a Cancer-Predisposing Syndrome that affects patients with germline RET mutations. Animal models do not faithfully recapitulate the full clinical spectrum of the disease. Moreover, it has been suggested that primitive malignant stem cells could be at the origin of resistances and relapses in patients treated with standard chemotherapy. In order to modelling MEN2A malignant primitive stem cells, we have induced to pluripotency MEN2A peripheral blood mononuclear cells from patients who developed medullary thyroid carcinoma harboring “high risk” or “moderate risk” RET mutation. Methods PBMC from patients with germline RETC620R and RetC634Y mutations were reprogrammed into pluripotent stem cells using Sendai-virus mediated Oct4, Sox2, Klf4 and c-Myc gene transfer. An isogenic IPSC line was generated by genome editing, using CRISPR-Cas9 to correct the “high risk” RETC634Y mutation. Hallmarks of pluripotency, genotype and phenotypes were characterized. Results Pluripotency behaviour of each IPSC line was confirmed in vitro (EBs, and pluripotent markers) and in vivo (teratoma assay in immunodeficient mice). Genome edition of the RETC634Y iPSC led to the generation of the RETY634C isogenic control iPSC. Ret expression was confirmed on both RETC634Y and RETY634C. In order to determine the accuracy and absence of off-target effects, we have performed a whole exome sequencing of both RET-mutated and RET-corrected IPSCs. These experiments revealed some off target effects of the CRISPR-mediated gene edition. Gene-array datas revealed an increased expression of neuronal development-related set of genes in RETC634Y iPSC, as compared to RETY634C control, that may account for the development of certain MEN2A features. Treatment of IPSC with vandetanib, a Ret inhibitor, led to a decrease of iPSC colonies formation in RETC634Y mutated iPSC compared to RETY634C, suggesting that RET-iPSC could serve as a plateform drug screening model. The comprehensive pathological assessment of IPSC RET-mutated and corrected derived-teratoma did not reveal, at this point, any neuroendocrine tumor-reminiscent structure. Conclusion We report here the first MEN2A-iPSC from “high risk” RETC634Y iPSC and its genome-edited isogenic normal IPSC, with their genomic profiling by whole exome sequencing. These well caracterized RET-IPSC will allow to develop cell-based assays in high throughput screening for drug discovery and to model MEN2A. Citation Format: Julien Hadoux, Christophe Desterke, Olivier Feraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin Schlumberger, Annelise Bennaceur-Griscelli, Ali Turhan. Generation of patient-specific and genome-edited MEN2A patient-derived induced pluripotent stem cells as novel tools for drug screening. [abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA. Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr 2483.
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Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2A (MEN2A) Syndrome with RET mutation.
Stem cell research, 2016Co-Authors: Julien Hadoux, Olivier Feraud, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin Schlumberger, Annelise Bennaceur-griscelli, Ali G. TurhanAbstract:Multiple Endocrine Neoplasia Type 2B (MEN2B) is a Cancer-Predisposing Syndrome that affects patients with germline RET mutations. The clinical spectrum of the Syndrome includes medullary thyroid carcinoma (MTC) and pheochromocytoma. Currently, there is no satisfactory model recapitulating all the features of the disease especially at the level of stem cells. We generated induced pluripotent stem cells (iPSCs) from a patient with RET mutation at codon 918 who developed pheochromocytoma and MTC. These iPSC had normal karyotype, harboured the RETM918T mutation and expressed pluripotency hallmarks. A comprehensive pathological assessment of teratoma was performed after injection in immunodeficient mice.
