Revisiting fetal hemoglobin inducers in beta-hemoglobinopathies: a review of natural products, conventional and combinatorial therapies
- PMID: 34822068
- DOI: 10.1007/s11033-021-06977-8
Revisiting fetal hemoglobin inducers in beta-hemoglobinopathies: a review of natural products, conventional and combinatorial therapies
Abstract
Beta-hemoglobinopathies exhibit a heterogeneous clinical picture with varying degrees of clinical severity. Pertaining to the limited treatment options available, where blood transfusion still remains the commonest mode of treatment, pharmacological induction of fetal hemoglobin (HbF) has been a lucrative therapeutic intervention. Till now more than 70 different HbF inducers have been identified. The practical usage of many pharmacological drugs has been limited due to safety concerns. Natural compounds, like Resveratrol, Ripamycin and Bergaptene, with limited cytotoxicity and high efficacy have started capturing the attention of researchers. In this review, we have summarized pharmacological drugs and bioactive compounds isolated from natural sources that have been shown to increase HbF significantly. It primarily discusses recently identified synthetic and natural compounds, their mechanism of action, and their suitable screening platforms, including high throughput drug screening technology and biosensors. It also delves into the topic of combinatorial therapy and drug repurposing for HbF induction. Overall, we aim to provide insights into where we stand in HbF induction strategies for treating β-hemoglobinopathies.
Keywords: Beta-hemoglobinopathies; Chemotherapeutic drugs; Fetal hemoglobin regulation; Natural compounds; Pharmacological induction; Screening platforms.
© 2021. The Author(s), under exclusive licence to Springer Nature B.V.
Similar articles
-
Integrative microRNA and gene expression analysis identifies new drug repurposing candidates for fetal hemoglobin induction in β-hemoglobinopathies.Gene. 2019 Jul 20;706:77-83. doi: 10.1016/j.gene.2019.04.077. Epub 2019 Apr 29. Gene. 2019. PMID: 31048070
-
Natural Remedies for the Treatment of Beta-Thalassemia and Sickle Cell Anemia-Current Status and Perspectives in Fetal Hemoglobin Reactivation.Int Sch Res Notices. 2014 Oct 2;2014:123257. doi: 10.1155/2014/123257. eCollection 2014. Int Sch Res Notices. 2014. PMID: 27350962 Free PMC article. Review.
-
Fetal hemoglobin chemical inducers for treatment of hemoglobinopathies.Ann Hematol. 2009 Jun;88(6):505-28. doi: 10.1007/s00277-008-0637-y. Epub 2008 Nov 15. Ann Hematol. 2009. PMID: 19011856 Review.
-
Phthalides serve as potent modulators to boost fetal hemoglobin induction therapy for β-hemoglobinopathies.Blood Adv. 2019 May 14;3(9):1493-1498. doi: 10.1182/bloodadvances.2019031120. Blood Adv. 2019. PMID: 31072835 Free PMC article.
-
A cell stress signaling model of fetal hemoglobin induction: what doesn't kill red blood cells may make them stronger.Exp Hematol. 2008 Sep;36(9):1057-72. doi: 10.1016/j.exphem.2008.06.014. Exp Hematol. 2008. PMID: 18718415 Review.
Cited by
-
Pharmacological Induction of Fetal Hemoglobin in β-Thalassemia and Sickle Cell Disease: An Updated Perspective.Pharmaceuticals (Basel). 2022 Jun 16;15(6):753. doi: 10.3390/ph15060753. Pharmaceuticals (Basel). 2022. PMID: 35745672 Free PMC article. Review.
-
Relationship between hemoglobinopathies and male infertility: a scoping review.Int J Hematol. 2024 Nov;120(5):566-574. doi: 10.1007/s12185-024-03844-7. Epub 2024 Sep 27. Int J Hematol. 2024. PMID: 39331276 Free PMC article.
-
Effect of Resveratrol on Pregnancy, Prenatal Complications and Pregnancy-Associated Structure Alterations.Antioxidants (Basel). 2023 Jan 31;12(2):341. doi: 10.3390/antiox12020341. Antioxidants (Basel). 2023. PMID: 36829900 Free PMC article. Review.
-
Vitamin C derivative/AA2P promotes erythroid differentiation by upregulating CA1.Life Med. 2023 Nov 13;2(5):lnad043. doi: 10.1093/lifemedi/lnad043. eCollection 2023 Oct. Life Med. 2023. PMID: 39872895 Free PMC article.
-
Ferroptosis as an emerging target in sickle cell disease.Curr Res Toxicol. 2024 Jun 18;7:100181. doi: 10.1016/j.crtox.2024.100181. eCollection 2024. Curr Res Toxicol. 2024. PMID: 39021403 Free PMC article.
References
-
- Demirci S, Leonard A, Tisdale JF (2020) Genome editing strategies for fetal hemoglobin induction in beta-hemoglobinopathies. Hum Mol Genet 29:R100–R106. https://doi.org/10.1093/hmg/ddaa088 - DOI - PubMed - PMC
-
- Magrin E, Miccio A, Cavazzana M (2019) Lentiviral and genome-editing strategies for the treatment of β-hemoglobinopathies. Blood 134(15):1203–1213. https://doi.org/10.1182/blood.2019000949 - DOI - PubMed
-
- Vadolas J, Glaser A, McColl B (2015) The therapeutic potential of genome editing for β-thalassemia. F1000Research 4:1–10. https://doi.org/10.12688/f1000research.7087.1 - DOI
-
- Cao A, Galanello R (2010) Beta-thalassemia. Genet Med 12(2):61–76. https://doi.org/10.1097/GIM.0b013e3181cd68ed - DOI - PubMed
-
- Muncie HL, Campbell JS (2009) Alpha and beta thalassemia. Am Fam Physician 80(4):339–344 - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources