S. Barati, S. Mousavi, Jamal Motallebzadeh Khanmiri, Mohammad Khani-Eshratabdi
{"title":"CCDC26和FOXCUT基因在急性淋巴细胞白血病中的表达水平","authors":"S. Barati, S. Mousavi, Jamal Motallebzadeh Khanmiri, Mohammad Khani-Eshratabdi","doi":"10.22037/AMLS.V7.33294","DOIUrl":null,"url":null,"abstract":"Background and Aim: Acute lymphoblastic leukemia (ALL) is a malignant disease of lymphoid progenitor cells affecting both children and adults. Long non-coding RNAs (lncRNAs) are one kind of non-coding RNAs (ncRNAs), reported modulating the initiation or progression of diverse cancers. However, the role of CCDC26 and FOXCUT long non-coding RNAs in ALL has been unknown. In this study, we explored the expression of FOXCUT and CCDC26 lncRNAs in acute lymphoblastic leukemia cell lines. \nMethods: Acute T lymphoblastic leukemia cell lines, RPMI 8402, Jurkat, B lymphoblastic leukemia, Daudi, and Ramos cell lines were used. After culturing the cells, RNA extraction and cDNA synthesis were performed. The real-time PCR technique was then used to study the expression of CCDC26, FOXCUT, C-kit, and FOXC1 genes. \nResult: We found a significant increase of CCDC26 expression in RPMI 8402 (p <0.0001) and Ramos (p <0.05) cell lines compared to the control, while decreased expression of these genes was observed in Jurkat and Daudi cell lines. Furthermore, FOXCUT gene had a significant increase in expression in all cell lines compared to the control (p <0.01 in Daudi and RPMI 8402 cell lines) (p <0.001 in Jurkat and Ramos cell lines). \nConclusion: Our results demonstrated that CCDC26 and FOXCUT genes can play a regulatory role in acute lymphoblastic leukemia and may serve as a potential diagnostic biomarker and therapeutic target of acute lymphoblastic leukemia. \n*Corresponding Author: Seyed Hadi Mousavi, Email: hmousavi@tums.ac.ir; \nORCID: https://orcid.org/0000-0002-4686-5232 \nPlease cite this article as: Barati S, Mousavi SH, Motallebzadeh-Khanmiri J, Khani-Eshratabdi M. The Expression Level of CCDC26 and FOXCUT Genes in Acute Lymphoblastic Leukemia. Arch Med Lab Sci. 2021;7:1-9 (e16). https://doi.org/10.22037/amls.v7.33294","PeriodicalId":18401,"journal":{"name":"Medical laboratory sciences","volume":"28 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Expression Level of CCDC26 and FOXCUT Genes in Acute Lymphoblastic Leukemia\",\"authors\":\"S. Barati, S. Mousavi, Jamal Motallebzadeh Khanmiri, Mohammad Khani-Eshratabdi\",\"doi\":\"10.22037/AMLS.V7.33294\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background and Aim: Acute lymphoblastic leukemia (ALL) is a malignant disease of lymphoid progenitor cells affecting both children and adults. Long non-coding RNAs (lncRNAs) are one kind of non-coding RNAs (ncRNAs), reported modulating the initiation or progression of diverse cancers. However, the role of CCDC26 and FOXCUT long non-coding RNAs in ALL has been unknown. In this study, we explored the expression of FOXCUT and CCDC26 lncRNAs in acute lymphoblastic leukemia cell lines. \\nMethods: Acute T lymphoblastic leukemia cell lines, RPMI 8402, Jurkat, B lymphoblastic leukemia, Daudi, and Ramos cell lines were used. After culturing the cells, RNA extraction and cDNA synthesis were performed. The real-time PCR technique was then used to study the expression of CCDC26, FOXCUT, C-kit, and FOXC1 genes. \\nResult: We found a significant increase of CCDC26 expression in RPMI 8402 (p <0.0001) and Ramos (p <0.05) cell lines compared to the control, while decreased expression of these genes was observed in Jurkat and Daudi cell lines. Furthermore, FOXCUT gene had a significant increase in expression in all cell lines compared to the control (p <0.01 in Daudi and RPMI 8402 cell lines) (p <0.001 in Jurkat and Ramos cell lines). \\nConclusion: Our results demonstrated that CCDC26 and FOXCUT genes can play a regulatory role in acute lymphoblastic leukemia and may serve as a potential diagnostic biomarker and therapeutic target of acute lymphoblastic leukemia. \\n*Corresponding Author: Seyed Hadi Mousavi, Email: hmousavi@tums.ac.ir; \\nORCID: https://orcid.org/0000-0002-4686-5232 \\nPlease cite this article as: Barati S, Mousavi SH, Motallebzadeh-Khanmiri J, Khani-Eshratabdi M. The Expression Level of CCDC26 and FOXCUT Genes in Acute Lymphoblastic Leukemia. Arch Med Lab Sci. 2021;7:1-9 (e16). https://doi.org/10.22037/amls.v7.33294\",\"PeriodicalId\":18401,\"journal\":{\"name\":\"Medical laboratory sciences\",\"volume\":\"28 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-10-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical laboratory sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.22037/AMLS.V7.33294\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical laboratory sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22037/AMLS.V7.33294","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The Expression Level of CCDC26 and FOXCUT Genes in Acute Lymphoblastic Leukemia
Background and Aim: Acute lymphoblastic leukemia (ALL) is a malignant disease of lymphoid progenitor cells affecting both children and adults. Long non-coding RNAs (lncRNAs) are one kind of non-coding RNAs (ncRNAs), reported modulating the initiation or progression of diverse cancers. However, the role of CCDC26 and FOXCUT long non-coding RNAs in ALL has been unknown. In this study, we explored the expression of FOXCUT and CCDC26 lncRNAs in acute lymphoblastic leukemia cell lines.
Methods: Acute T lymphoblastic leukemia cell lines, RPMI 8402, Jurkat, B lymphoblastic leukemia, Daudi, and Ramos cell lines were used. After culturing the cells, RNA extraction and cDNA synthesis were performed. The real-time PCR technique was then used to study the expression of CCDC26, FOXCUT, C-kit, and FOXC1 genes.
Result: We found a significant increase of CCDC26 expression in RPMI 8402 (p <0.0001) and Ramos (p <0.05) cell lines compared to the control, while decreased expression of these genes was observed in Jurkat and Daudi cell lines. Furthermore, FOXCUT gene had a significant increase in expression in all cell lines compared to the control (p <0.01 in Daudi and RPMI 8402 cell lines) (p <0.001 in Jurkat and Ramos cell lines).
Conclusion: Our results demonstrated that CCDC26 and FOXCUT genes can play a regulatory role in acute lymphoblastic leukemia and may serve as a potential diagnostic biomarker and therapeutic target of acute lymphoblastic leukemia.
*Corresponding Author: Seyed Hadi Mousavi, Email: hmousavi@tums.ac.ir;
ORCID: https://orcid.org/0000-0002-4686-5232
Please cite this article as: Barati S, Mousavi SH, Motallebzadeh-Khanmiri J, Khani-Eshratabdi M. The Expression Level of CCDC26 and FOXCUT Genes in Acute Lymphoblastic Leukemia. Arch Med Lab Sci. 2021;7:1-9 (e16). https://doi.org/10.22037/amls.v7.33294