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  1. Article ; Online: Cardiomyocyte DNA Damage Predicts Functional Recovery in Heart Failure Patients.

    Ali, Shah R / Sadek, Hesham A

    JACC. Heart failure

    2024  Volume 12, Issue 4, Page(s) 662–664

    MeSH term(s) Humans ; Heart Failure ; Myocytes, Cardiac ; Apoptosis ; DNA Damage
    Language English
    Publishing date 2024-02-26
    Publishing country United States
    Document type Editorial
    ZDB-ID 2705621-1
    ISSN 2213-1787 ; 2213-1779
    ISSN (online) 2213-1787
    ISSN 2213-1779
    DOI 10.1016/j.jchf.2024.01.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: WNT links metabolism and cell cycle in postnatal cardiomyocytes.

    Menendez-Montes, Ivan / Sadek, Hesham A

    The journal of cardiovascular aging

    2022  Volume 2, Issue 2

    Language English
    Publishing date 2022-04-18
    Publishing country United States
    Document type Journal Article
    ISSN 2768-5993
    ISSN (online) 2768-5993
    DOI 10.20517/jca.2022.18
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Experimental Hypoxia as a Model for Cardiac Regeneration in Mice.

    Nakada, Yuji / Sadek, Hesham A

    Methods in molecular biology (Clifton, N.J.)

    2020  Volume 2158, Page(s) 337–344

    Abstract: Experimental hypoxia has been used for decades to examine the adaptive response to low-oxygen environments. Various models have been studied, including flies, worms, fish, rodents, and humans. Our lab has recently used this technology to examine the ... ...

    Abstract Experimental hypoxia has been used for decades to examine the adaptive response to low-oxygen environments. Various models have been studied, including flies, worms, fish, rodents, and humans. Our lab has recently used this technology to examine the effect of environmental hypoxia on mammalian heart regeneration. In this chapter, we describe studies of systemic hypoxia in mice. We found that systemic hypoxia can blunt oxidative DNA damage and induce cardiomyocyte proliferation. While our primary interests are focused on cardiovascular research, these hypoxia protocols are applicable to any other organ system.
    MeSH term(s) Animals ; Atmosphere Exposure Chambers ; Calibration ; Heart/physiopathology ; Hypoxia/blood ; Hypoxia/physiopathology ; Mice ; Models, Animal ; Myocytes, Cardiac/metabolism ; Oxygen/metabolism ; Regeneration/physiology
    Chemical Substances Oxygen (S88TT14065)
    Language English
    Publishing date 2020-08-28
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-0716-0668-1_25
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Neonatal heart regeneration: Moving from phenomenology to regenerative medicine.

    Sadek, Hesham A / Porrello, Enzo R

    The Journal of thoracic and cardiovascular surgery

    2020  Volume 159, Issue 6, Page(s) 2451–2455

    MeSH term(s) Animals ; Animals, Newborn ; Cell Proliferation ; Diffusion of Innovation ; Forecasting ; Heart Failure/metabolism ; Heart Failure/pathology ; Heart Failure/physiopathology ; Heart Failure/surgery ; Humans ; Infant, Newborn ; Myocardium/metabolism ; Myocardium/pathology ; Recovery of Function ; Regeneration ; Regenerative Medicine/trends ; Signal Transduction ; Thyroid Hormones/metabolism ; Tissue Engineering/trends
    Chemical Substances Thyroid Hormones
    Language English
    Publishing date 2020-02-19
    Publishing country United States
    Document type Editorial ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 3104-5
    ISSN 1097-685X ; 0022-5223
    ISSN (online) 1097-685X
    ISSN 0022-5223
    DOI 10.1016/j.jtcvs.2019.11.140
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Hypoxia Induces Cardiomyocyte Proliferation in Humans.

    Ahmed, Mahmoud S / Sadek, Hesham A

    JACC. Basic to translational science

    2020  Volume 5, Issue 5, Page(s) 461–462

    Language English
    Publishing date 2020-05-25
    Publishing country United States
    Document type Editorial ; Comment
    ISSN 2452-302X
    ISSN (online) 2452-302X
    DOI 10.1016/j.jacbts.2020.04.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Metabolic Control of Cardiomyocyte Cell Cycle.

    Menendez-Montes, Ivan / Garry, Daniel J / Zhang, Jianyi Jay / Sadek, Hesham A

    Methodist DeBakey cardiovascular journal

    2023  Volume 19, Issue 5, Page(s) 26–36

    Abstract: Current therapies for heart failure aim to prevent the deleterious remodeling that occurs after MI injury, but currently no therapies are available to replace lost cardiomyocytes. Several organisms now being studied are capable of regenerating their ... ...

    Abstract Current therapies for heart failure aim to prevent the deleterious remodeling that occurs after MI injury, but currently no therapies are available to replace lost cardiomyocytes. Several organisms now being studied are capable of regenerating their myocardium by the proliferation of existing cardiomyocytes. In this review, we summarize the main metabolic pathways of the mammalian heart and how modulation of these metabolic pathways through genetic and pharmacological approaches influences cardiomyocyte proliferation and heart regeneration.
    MeSH term(s) Animals ; Humans ; Myocytes, Cardiac/metabolism ; Cell Proliferation ; Myocardium/metabolism ; Heart Failure/therapy ; Heart Failure/metabolism ; Cell Cycle ; Regeneration/genetics ; Mammals
    Language English
    Publishing date 2023-11-16
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2544079-2
    ISSN 1947-6108 ; 1947-6108
    ISSN (online) 1947-6108
    ISSN 1947-6108
    DOI 10.14797/mdcvj.1309
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Networks that Govern Cardiomyocyte Proliferation to Facilitate Repair of the Injured Mammalian Heart.

    Garry, Daniel J / Zhang, Jianyi Jay / Larson, Thijs A / Sadek, Hesham A / Garry, Mary G

    Methodist DeBakey cardiovascular journal

    2023  Volume 19, Issue 5, Page(s) 16–25

    Abstract: Cardiovascular diseases are the number one cause of death worldwide and in the United States (US). Cardiovascular diseases frequently progress to end-stage heart failure, and curative therapies are extremely limited. Intense interest has focused on ... ...

    Abstract Cardiovascular diseases are the number one cause of death worldwide and in the United States (US). Cardiovascular diseases frequently progress to end-stage heart failure, and curative therapies are extremely limited. Intense interest has focused on deciphering the cascades and networks that govern cardiomyocyte proliferation and regeneration of the injured heart. For example, studies have shown that lower organisms such as the adult newt and adult zebrafish have the capacity to completely regenerate their injured heart with restoration of function. Similarly, the neonatal mouse and pig are also able to completely regenerate injured myocardium due to cardiomyocyte proliferation from preexisting cardiomyocytes. Using these animal models and transcriptome analyses, efforts have focused on the definition of factors and signaling pathways that can reactivate and induce cardiomyocyte proliferation in the adult mammalian injured heart. These studies and discoveries have the potential to define novel therapies to promote cardiomyocyte proliferation and repair of the injured, mammalian heart.
    MeSH term(s) Animals ; Mice ; Cell Proliferation ; Mammals ; Myocardial Infarction ; Myocardium/metabolism ; Myocytes, Cardiac/metabolism ; Regeneration/physiology ; Swine ; Zebrafish
    Language English
    Publishing date 2023-11-16
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2544079-2
    ISSN 1947-6108 ; 1947-6108
    ISSN (online) 1947-6108
    ISSN 1947-6108
    DOI 10.14797/mdcvj.1300
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Neonatal Heart Regeneration: Comprehensive Literature Review.

    Lam, Nicholas T / Sadek, Hesham A

    Circulation

    2018  Volume 138, Issue 4, Page(s) 412–423

    Abstract: Background: The adult mammalian heart is incapable of meaningful functional recovery after injury, and thus promoting heart regeneration is 1 of the most important therapeutic targets in cardiovascular medicine. In contrast to the adult mammalian heart, ...

    Abstract Background: The adult mammalian heart is incapable of meaningful functional recovery after injury, and thus promoting heart regeneration is 1 of the most important therapeutic targets in cardiovascular medicine. In contrast to the adult mammalian heart, the neonatal mammalian heart is capable of regeneration after various types of injury. Since the first report in 2011, a number of groups have reported their findings on neonatal heart regeneration. The current review provides a comprehensive analysis of heart regeneration studies in neonatal mammals conducted to date, outlines lessons learned, and poses unanswered questions.
    Methods: We performed a PubMed search using the keywords "neonatal" and "heart" and "regeneration." In addition, we assessed all publications that cited the first neonatal heart regeneration reports: Porrello et al, Science, Feb 2011 for apical resection injury; Porrello et al, PNAS, Dec 2012 for coronary ligation injury; and Mahmoud et al, Nature Methods, Jan 2014 for surgical methodology. Publications were examined for surgical models used, timing of surgery, and postinjury assessment including anatomic, histological, and functional assessment, as well as conclusions drawn.
    Results: We found 30 publications that performed neonatal apical resection, 19 publications that performed neonatal myocardial infarction by coronary artery ligation, and 6 publications that performed cryoinjury using liquid nitrogen-cooled metal probes. Both apical resection and ischemic infarction injury in neonatal mice result in a robust regenerative response, mediated by cardiomyocyte proliferation. On the other hand, several reports have demonstrated that cryoinjury is associated with incomplete heart regeneration in neonatal mice. Not surprisingly, several studies suggest that injury size, as well as surgical and histological techniques, can strongly influence the observed regenerative response and final conclusions. Studies have utilized these neonatal cardiac injury models to identify factors that either inhibit or stimulate heart regeneration.
    Conclusions: Overall, there is consensus that both apical resection and coronary ligation injuries during the first 2 days of life result in heart regeneration in neonatal mammals, whereas cryoinjury was not associated with a similar regenerative response. This regenerative response is mediated by proliferation of preexisting cardiomyocytes, and is modifiable by injury size and surgical technique, as well as metabolic, immunologic, genetic, and environmental factors.
    MeSH term(s) Animals ; Animals, Newborn ; Cell Proliferation ; Disease Models, Animal ; Heart/physiopathology ; Heart Injuries/metabolism ; Heart Injuries/pathology ; Heart Injuries/physiopathology ; Humans ; Infant, Newborn ; Mice ; Myocardial Infarction/metabolism ; Myocardial Infarction/pathology ; Myocardial Infarction/physiopathology ; Myocytes, Cardiac/metabolism ; Myocytes, Cardiac/pathology ; Recovery of Function ; Regeneration ; Signal Transduction
    Language English
    Publishing date 2018-12-20
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 80099-5
    ISSN 1524-4539 ; 0009-7322 ; 0069-4193 ; 0065-8499
    ISSN (online) 1524-4539
    ISSN 0009-7322 ; 0069-4193 ; 0065-8499
    DOI 10.1161/CIRCULATIONAHA.118.033648
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Mechanisms of Neonatal Heart Regeneration.

    Cardoso, Alisson C / Pereira, Ana Helena M / Sadek, Hesham A

    Current cardiology reports

    2020  Volume 22, Issue 5, Page(s) 33

    Abstract: Purpose of review: This review provides an overview of the molecular mechanisms underpinning the cardiac regenerative capacity during the neonatal period and the potential targets for developing novel therapies to restore myocardial loss.: Recent ... ...

    Abstract Purpose of review: This review provides an overview of the molecular mechanisms underpinning the cardiac regenerative capacity during the neonatal period and the potential targets for developing novel therapies to restore myocardial loss.
    Recent findings: We present recent advances in the understanding of the molecular mechanisms of neonatal cardiac regeneration and the implications for the development of new cardiac regenerative therapies. During the early postnatal period, several cell types and pathways are involved in cardiomyocyte proliferation including immune response, nerve signaling, extracellular matrix, mitochondria substrate utilization, gene expression, miRNAs, and cell cycle progression. The early neonatal mammalian heart has remarkable regenerative capacity, which is mediated by proliferation of endogenous cardiomyocytes, and is lost when cardiomyocytes stop dividing shortly after birth. A wide array of mechanisms that regulate this regenerative process have been proposed.
    MeSH term(s) Cell Proliferation/physiology ; Heart ; Humans ; Infant, Newborn ; Myocardium ; Myocytes, Cardiac/physiology ; Regeneration/physiology ; Regenerative Medicine/methods ; Regenerative Medicine/trends ; Signal Transduction
    Language English
    Publishing date 2020-04-24
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2055373-0
    ISSN 1534-3170 ; 1523-3782
    ISSN (online) 1534-3170
    ISSN 1523-3782
    DOI 10.1007/s11886-020-01282-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Hypoxia-induced stabilization of HIF2A promotes cardiomyocyte proliferation by attenuating DNA damage.

    Ali, Shah R / Nguyen, Ngoc Uyen Nhi / Menendez-Montes, Ivan / Hsu, Ching-Cheng / Elhelaly, Waleed / Lam, Nicholas T / Li, Shujuan / Elnwasany, Abdallah / Nakada, Yuji / Thet, Suwannee / Foo, Roger S Y / Sadek, Hesham A

    The journal of cardiovascular aging

    2024  Volume 4, Issue 1

    Abstract: Introduction: Gradual exposure to a chronic hypoxic environment leads to cardiomyocyte proliferation and improved cardiac function in mouse models through a reduction in oxidative DNA damage. However, the upstream transcriptional events that link ... ...

    Abstract Introduction: Gradual exposure to a chronic hypoxic environment leads to cardiomyocyte proliferation and improved cardiac function in mouse models through a reduction in oxidative DNA damage. However, the upstream transcriptional events that link chronic hypoxia to DNA damage have remained obscure.
    Aim: We sought to determine whether hypoxia signaling mediated by the hypoxia-inducible factor 1 or 2 (HIF1A or HIF2A) underlies the proliferation phenotype that is induced by chronic hypoxia.
    Methods and results: We used genetic loss-of-function models using cardiomyocyte-specific HIF1A and HIF2A gene deletions in chronic hypoxia. We additionally characterized a cardiomyocyte-specific HIF2A overexpression mouse model in normoxia during aging and upon injury. We performed transcriptional profiling with RNA-sequencing on cardiac tissue, from which we verified candidates at the protein level. We find that HIF2A - rather than HIF1A - mediates hypoxia-induced cardiomyocyte proliferation. Ectopic, oxygen-insensitive HIF2A expression in cardiomyocytes reveals the cell-autonomous role of HIF2A in cardiomyocyte proliferation. HIF2A overexpression in cardiomyocytes elicits cardiac regeneration and improvement in systolic function after myocardial infarction in adult mice. RNA-sequencing reveals that ectopic HIF2A expression attenuates DNA damage pathways, which was confirmed with immunoblot and immunofluorescence.
    Conclusion: Our study provides mechanistic insights about a new approach to induce cardiomyocyte renewal and mitigate cardiac injury in the adult mammalian heart. In light of evidence that DNA damage accrues in cardiomyocytes with aging, these findings may help to usher in a new therapeutic approach to overcome such age-related changes and achieve regeneration.
    Language English
    Publishing date 2024-01-29
    Publishing country United States
    Document type Journal Article
    ISSN 2768-5993
    ISSN (online) 2768-5993
    DOI 10.20517/jca.2023.43
    Database MEDical Literature Analysis and Retrieval System OnLINE

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