4.7 Article

Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1

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出版社

MDPI
DOI: 10.3390/ijms20081938

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circular RNA; alternative splicing; muscular dystrophies

资金

  1. Telethon-Italy [GGP16213]
  2. AFM-Telethon [18477]
  3. Ministero della Salute [RF-2011-02347907, PE-2011-02348537]
  4. ERC-2013 [AdG 340172-MUNCODD]
  5. Fondazione Roma
  6. FMM-Fondazione Malattie Miotoniche
  7. Ministero della Salute (5 x 1000)

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Circular RNAs (circRNAs) constitute a recently re-discovered class of non-coding RNAs functioning as sponges for miRNAs and proteins, affecting RNA splicing and regulating transcription. CircRNAs are generated by back-splicing, which is the linking covalently of 3- and 5-ends of exons. Thus, circRNA levels might be deregulated in conditions associated with altered RNA-splicing. Significantly, growing evidence indicates their role in human diseases. Specifically, myotonic dystrophy type 1 (DM1) is a multisystemic disorder caused by expanded CTG repeats in the DMPK gene which results in abnormal mRNA-splicing. In this investigation, circRNAs expressed in DM1 skeletal muscles were identified by analyzing RNA-sequencing data-sets followed by qPCR validation. In muscle biopsies, out of nine tested, four transcripts showed an increased circular fraction: CDYL, HIPK3, RTN4_03, and ZNF609. Their circular fraction values correlated with skeletal muscle strength and with splicing biomarkers of disease severity, and displayed higher values in more severely affected patients. Moreover, Receiver-Operating-Characteristics curves of these four circRNAs discriminated DM1 patients from controls. The identified circRNAs were also detectable in peripheral-blood-mononuclear-cells (PBMCs) and the plasma of DM1 patients, but they were not regulated significantly. Finally, increased circular fractions of RTN4_03 and ZNF609 were also observed in differentiated myogenic cell lines derived from DM1 patients. In conclusion, this pilot study identified circRNA dysregulation in DM1 patients.

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Morisue, Y. Moriwaki, B. Mours, C. M. Mow-Lowry, S. Mozzon, F. Muciaccia, Arunava Mukherjee, D. Mukherjee, Soma Mukherjee, Subroto Mukherjee, Suvodip Mukherjee, N. Mukund, A. Mullavey, J. Munch, E. A. Muniz, P. G. Murray, R. Musenich, S. Muusse, S. L. Nadji, K. Nagano, A. Nagar, K. Nakamura, H. Nakano, M. Nakano, Y. Nakayama, V Napolano, I Nardecchia, T. Narikawa, H. Narola, L. Naticchioni, B. Nayak, R. K. Nayak, B. F. Neil, J. Neilson, A. Nelson, T. J. N. Nelson, M. Nery, P. Neubauer, A. Neunzert, K. Y. Ng, S. W. S. Ng, C. Nguyen, P. Nguyen, T. Nguyen, L. NguyenQuynh, J. Ni, W-T Ni, S. A. Nichols, T. Nishimoto, A. Nishizawa, S. Nissanke, E. Nitoglia, F. Nocera, M. Norman, C. North, S. Nozaki, G. Nurbek, L. K. Nuttall, Y. Obayashi, J. Oberling, B. D. O'Brien, J. O'Dell, E. Oelker, W. Ogaki, G. Oganesyan, J. J. Oh, K. Oh, S. H. Oh, M. Ohashi, T. Ohashi, M. Ohkawa, F. Ohme, H. Ohta, M. A. Okada, Y. Okutani, C. Olivetto, K. Oohara, R. Oram, B. O'Reilly, R. G. Ormiston, N. D. Ormsby, R. O'Shaughnessy, E. O'Shea, S. Oshino, S. Ossokine, C. Osthelder, S. Otabe, D. J. Ottaway, H. Overmier, A. E. Pace, G. Pagano, R. Pagano, M. A. Page, G. Pagliaroli, A. Pai, S. A. Pai, S. Pal, J. R. Palamos, O. Palashov, C. Palomba, H. Pan, K-C Pan, P. K. Panda, P. T. H. Pang, C. Pankow, F. Pannarale, B. C. Pant, F. H. Panther, F. Paoletti, A. Paoli, A. Paolone, G. Pappas, A. Parisi, H. Park, J. Park, W. Parker, D. Pascucci, A. Pasqualetti, R. Passaquieti, D. Passuello, M. Patel, M. Pathak, B. Patricelli, A. S. Patron, S. Paul, E. Payne, M. Pedraza, R. Pedurand, M. Pegoraro, A. Pele, F. E. Pena Arellano, S. Penano, S. Penn, A. Perego, A. Pereira, T. Pereira, C. J. Perez, C. Perigois, C. C. Perkins, A. Perreca, S. Perries, D. Pesios, J. Petermann, D. Petterson, H. P. Pfeiffer, H. Pham, K. A. Pham, K. S. Phukon, H. Phurailatpam, O. J. Piccinni, M. Pichot, M. Piendibene, F. Piergiovanni, L. Pierini, V Pierro, G. Pillant, M. Pillas, F. Pilo, L. Pinard, C. Pineda-Bosque, I. M. Pinto, M. Pinto, B. J. Piotrzkowski, K. Piotrzkowski, M. Pirello, M. D. Pitkin, A. Placidi, E. Placidi, M. L. Planas, W. Plastino, C. Pluchar, R. Poggiani, E. Polini, D. Y. T. Pong, S. Ponrathnam, E. K. Porter, R. Poulton, A. Poverman, J. Powell, M. Pracchia, T. Pradier, A. K. Prajapati, K. Prasai, R. Prasanna, G. Pratten, M. Principe, G. A. Prodi, L. Prokhorov, P. Prosposito, L. Prudenzi, A. Puecher, M. Punturo, F. Puosi, P. Puppo, M. Puerrer, H. Qi, N. Quartey, V Quetschke, P. J. Quinonez, R. Quitzow-James, F. J. Raab, G. Raaijmakers, H. Radkins, N. Radulesco, P. Raffai, S. X. Rail, S. Raja, C. Rajan, K. E. Ramirez, T. D. Ramirez, A. Ramos-Buades, J. Rana, P. Rapagnani, A. Ray, V Raymond, N. Raza, M. Razzano, J. Read, L. A. Rees, T. Regimbau, L. Rei, S. Reid, S. W. Reid, D. H. Reitze, P. Relton, A. Renzini, P. Rettegno, B. Revenu, A. Reza, M. Rezac, F. Ricci, D. Richards, J. W. Richardson, L. Richardson, G. Riemenschneider, K. Riles, S. Rinaldi, K. Rink, N. A. Robertson, R. Robie, F. Robinet, A. Rocchi, S. Rodriguez, L. Rolland, J. G. Rollins, M. Romanelli, R. Romano, C. L. Romel, A. Romero, I. M. Romero-Shaw, J. H. Romie, S. Ronchini, L. Rosa, C. A. Rose, M. P. Ross, S. Rowan, S. J. Rowlinson, S. Roy, Santosh Roy, Soumen Roy, D. Rozza, P. Ruggi, K. Ruiz-Rocha, K. Ryan, S. Sachdev, T. Sadecki, J. Sadiq, S. Saha, Y. Saito, K. Sakai, M. Sakellariadou, S. Sakon, O. S. Salafia, F. Salces-Carcoba, L. Salconi, M. Saleem, F. Salemi, A. Samajdar, E. J. Sanchez, J. H. Sanchez, L. E. Sanchez, N. Sanchis-Gual, J. R. Sanders, A. Sanuy, T. R. Saravanan, N. Sarin, B. Sassolas, H. Satari, O. Sauter, R. L. Savage, V Savant, T. Sawada, H. L. Sawant, S. Sayah, D. Schaetzl, M. Scheel, J. Scheuer, M. G. Schiworski, P. Schmidt, S. Schmidt, R. Schnabel, M. Schneewind, R. M. S. Schofield, A. Schoenbeck, B. W. Schulte, B. F. Schutz, E. Schwartz, J. Scott, S. M. Scott, M. Seglar-Arroyo, Y. Sekiguchi, D. Sellers, A. S. Sengupta, D. Sentenac, E. G. Seo, V Sequino, A. Sergeev, Y. Setyawati, T. Shaffer, M. S. Shahriar, M. A. Shaikh, B. Shams, L. Shao, A. Sharma, P. Sharma, P. Shawhan, N. S. Shcheblanov, A. Sheela, Y. Shikano, M. Shikauchi, H. Shimizu, K. Shimode, H. Shinkai, T. Shishido, A. Shoda, D. H. Shoemaker, D. M. Shoemaker, S. ShyamSundar, M. Sieniawska, D. Sigg, L. Silenzi, L. P. Singer, D. Singh, M. K. Singh, N. Singh, A. Singha, A. M. Sintes, V Sipala, V Skliris, B. J. J. Slagmolen, T. J. Slaven-Blair, J. Smetana, J. R. Smith, L. Smith, R. J. E. Smith, J. Soldateschi, S. N. Somala, K. Somiya, I Song, K. Soni, S. Soni, V Sordini, F. Sorrentino, N. Sorrentino, R. Soulard, T. Souradeep, E. Sowell, V Spagnuolo, A. P. Spencer, M. Spera, P. Spinicelli, A. K. Srivastava, V Srivastava, K. Staats, C. Stachie, F. Stachurski, D. A. Steer, J. Steinlechner, S. Steinlechner, N. Stergioulas, D. J. Stops, M. Stover, K. A. Strain, L. C. Strang, G. Stratta, M. D. Strong, A. Strunk, R. Sturani, A. L. Stuver, M. Suchenek, S. Sudhagar, V Sudhir, R. Sugimoto, H. G. Suh, A. G. Sullivan, T. Z. Summerscales, L. Sun, S. Sunil, A. Sur, J. Suresh, P. J. Sutton, Takamasa Suzuki, Takanori Suzuki, Toshikazu Suzuki, B. L. Swinkels, P. Szewczyk, M. Tacca, H. Tagoshi, S. C. Tait, H. Takahashi, R. Takahashi, S. Takano, H. Takeda, M. Takeda, C. J. Talbot, C. Talbot, K. Tanaka, Taiki Tanaka, Takahiro Tanaka, A. J. Tanasijczuk, S. Tanioka, D. B. Tanner, D. Tao, L. Tao, R. D. Tapia, E. N. TapiaSanMartin, C. Taranto, A. Taruya, J. D. Tasson, R. Tenorio, J. E. S. Terhune, L. Terkowski, M. P. Thirugnanasambandam, M. Thomas, P. Thomas, E. E. Thompson, J. E. Thompson, S. R. Thondapu, K. A. Thorne, E. Thrane, Shubhanshu Tiwari, Srishti Tiwari, V Tiwari, A. M. Toivonen, A. E. Tolley, T. Tomaru, T. Tomura, M. Tonelli, Z. Tornasi, A. Torres-Forne, C. Torrie, I. Tosta E. Melo, D. Toyra, A. Trapananti, F. Travasso, G. Traylor, M. Trevor, M. C. Tringali, A. Tripathee, L. Troiano, A. Trovato, L. Trozzo, R. J. Trudeau, D. Tsai, K. W. Tsang, T. Tsang, J-S Tsao, M. Tse, R. Tso, S. Tsuchida, L. Tsukada, D. Tsuna, T. Tsutsui, K. Turbang, M. Turconi, D. Tuyenbayev, A. S. Ubhi, N. Uchikata, T. Uchiyama, R. P. Udall, A. Ueda, T. Uehara, K. Ueno, G. Ueshima, C. S. Unnikrishnan, A. L. Urban, T. Ushiba, A. Utina, G. Vajente, A. Vajpeyi, G. Valdes, M. Valentini, V. Valsan, N. VanBakel, M. VanBeuzekom, M. VanDael, J. F. J. van den Brand, C. Van den Broeck, D. C. Vander-Hyde, H. van Haevermaet, J. V. Van Heijningen, M. H. P. M. Van Putten, N. van Remortel, M. Vardaro, A. F. Vargas, V. Varma, M. Vasuth, A. Vecchio, G. Vedovato, J. Veitch, P. J. Veitch, J. Venneberg, G. Venugopalan, D. Verkindt, P. Verma, Y. Verma, S. M. Vermeulen, D. Veske, F. Vetrano, A. Vicere, S. Vidyant, A. D. Viets, A. Vijaykumar, V. Villa-Ortega, J-Y Vinet, A. Virtuoso, S. Vitale, H. Vocca, E. R. G. VonReis, J. S. A. von Wrangel, C. Vorvick, S. P. Vyatchanin, L. E. Wade, M. Wade, K. J. Wagner, R. C. Walet, M. Walker, G. S. Wallace, L. Wallace, J. Wang, J. Z. Wang, W. H. Wang, R. L. Ward, J. Warner, M. Was, T. Washimi, N. Y. Washington, J. Watchi, B. Weaver, C. R. Weaving, S. A. Webster, M. Weinert, A. J. Weinstein, R. Weiss, C. M. Weller, R. A. Weller, F. Wellmann, L. Wen, P. Wessels, K. Wette, J. T. Whelan, D. D. White, B. F. Whiting, C. Whittle, D. Wilken, D. Williams, M. J. Williams, A. R. Williamson, J. L. Willis, B. Willke, D. J. Wilson, C. C. Wipf, T. Wlodarczyk, G. Woan, J. Woehler, J. K. Wofford, D. Wong, I. C. F. Wong, M. Wright, C. Wu, D. S. Wu, H. Wu, D. M. Wysocki, L. Xiao, T. Yamada, H. Yamamoto, K. Yamamoto, T. Yamamoto, K. Yamashita, R. Yamazaki, F. W. Yang, K. Z. Yang, L. Yang, Y-C Yang, Y. Yang, Yang Yang, M. J. Yap, D. W. Yeeles, S-W Yeh, A. B. Yelikar, M. Ying, J. Yokoyama, T. Yokozawa, J. Yoo, T. Yoshioka, Hang Yu, Haocun Yu, H. Yuzurihara, M. Zanolin, S. Zeidler, T. Zelenova, J-P Zendri, M. Zevin, M. Zhan, H. Zhang, J. Zhang, L. Zhang, R. Zhang, T. Zhang, Y. Zhang, C. Zhao, G. Zhao, Y. Zhao, Yue Zhao, R. Zhou, Z. Zhou, X. J. Zhu, Z-H Zhu, A. B. Zimmerman, M. E. Zucker, J. Zweizig

Summary: We present the results of the first joint observation of the KAGRA detector with GEO600, demonstrating the feasibility and utility of KAGRA as a member of the global gravitational-wave detector network. The analysis includes the search for transient gravitational-wave signals and the evaluation of the network's sensitivity to various types of signals.

PROGRESS OF THEORETICAL AND EXPERIMENTAL PHYSICS (2022)

Editorial Material Cardiac & Cardiovascular Systems

Young at heart: a DNA methylation's tale

Alessia Mongelli, Antonella Farsetti, Carlo Gaetano

EUROPEAN HEART JOURNAL (2023)

Editorial Material Cell Biology

A guide to naming eukaryotic circular RNAs

Ling-Ling Chen, Albrecht Bindereif, Irene Bozzoni, Howard Y. Y. Chang, A. Gregory Matera, Myriam Gorospe, Thomas B. B. Hansen, Jorgen Kjems, Xu-Kai Ma, Jun Wei Pek, Nikolaus Rajewsky, Julia Salzman, Jeremy E. E. Wilusz, Li Yang, Fangqing Zhao

Summary: This Comment calls for a common nomenclature for naming circRNAs to ensure clarity and reproducibility in studies.

NATURE CELL BIOLOGY (2023)

Article Clinical Neurology

Clinical score for early diagnosis of myotonic dystrophy type 2

Vukan Ivanovic, Stojan Peric, Jovan Pesovic, Radoje Tubic, Ivo Bozovic, Ivana Petrovic Djordjevic, Dusanka Savic-Pavicevic, Giovanni Meola, Vidosava Rakocevic-Stojanovic

Summary: The study aims to determine the most indicative symptoms, signs, and diagnostic findings in patients referred to neurological outpatient units for suspicion of DM2. An easy-to-administer DM2 early diagnosis score (DM2-EDS) was developed for early diagnosis of DM2.

NEUROLOGICAL SCIENCES (2023)

Article Clinical Neurology

MBNL-dependent impaired development within the neuromuscular system in myotonic dystrophy type 1

Julie Tahraoui-Bories, Antoine Merien, Anchel Gonzalez-Barriga, Jeanne Laine, Celine Leteur, Helene Polveche, Alexandre Carteron, Juliette Duchesne De Lamotte, Camille Nicoleau, Jerome Polentes, Margot Jarrige, Mario Gomes-Pereira, Erwann Ventre, Pauline Poydenot, Denis Furling, Laurent Schaeffer, Claire Legay, Cecile Martinat

Summary: This study reveals the active involvement of motoneurons (MNs) in the pathogenesis of myotonic dystrophy type I (DM1). The researchers developed a functional neuromuscular model using DM1 and muscleblind protein (MBNL) knock-out human-induced pluripotent stem cell-derived MNs and healthy skeletal muscle cells. The study identified presynaptic defects and showed that the loss of RNA-binding MBNL proteins can reproduce these neuropathological defects. Comparative transcriptomic analyses also revealed common misregulation of neuronal-related processes in DM1. This approach has implications beyond DM1, as it can facilitate disease modeling studies and drug screening assays.

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2023)

Review Medicine, General & Internal

How epigenetics impacts on human diseases

Antonella Farsetti, Barbara Illi, Carlo Gaetano

Summary: Epigenetics is a rapidly growing field of biology that explores the impact of chemical modifications on DNA and associated proteins, which can profoundly influence gene expression, tissue development, and disease susceptibility. Understanding epigenetic changes is crucial for comprehending the role of environmental and lifestyle factors in health and disease, as well as intergenerational transmission of traits. Epigenetics has shown to be critical in various diseases and offers potential therapeutic avenues, but also comes with risks and unintended consequences that necessitate rigorous research for safe and effective interventions. This article provides a synthetic and historical overview of epigenetics and its significant achievements.

EUROPEAN JOURNAL OF INTERNAL MEDICINE (2023)

Article Chemistry, Inorganic & Nuclear

Exploring Rhenium Arene Piano-Stool Chemistry with [Re(η6-C6H6)(NCCH3)3]+: A Powerful Semi-Solvated Precursor

Robin Bolliger, Lukas Siebenmann, Emily Wolf, Megan Ross, Giuseppe Meola, Olivier Blacque, Henrik Braband, Roger Alberto

Summary: Thermal treatment of the Re-III hydride complex [ReH(eta(5)-C6H7)(eta(6)-C6H6)](+) in CH3CN results in the formation of [Re(eta(6)-C6H6)(NCCH3)(3)](+). This semi-solvated complex is remarkably stable under an ambient atmosphere and exhibits various substitution reactions with different ligands. The stability and reactivity of [Re(eta(6)-C6H6)(NCCH3)(3)](+) make it a promising candidate in various applications.

INORGANIC CHEMISTRY (2023)

Article Clinical Neurology

Myotonic dystrophy type 1 in the COVID-19 era

Jelena Ilic Zivojinovic, Katarina Djurdjevic, Ivo Bozovic, Giovanni Meola, Marina Peric, Ana Azanjac Arsic, Ivana Basta, Vidosava Rakocevic-Stojanovic, Stojan Peric

Summary: This cross-sectional study aimed to evaluate COVID-19 infection and vaccination rate in patients with myotonic dystrophy type 1 (DM1). The study found that 40.4% of DM1 patients were infected with COVID-19, with around 14% requiring hospitalization. Vaccination was highly effective in preventing severe COVID-19 cases, as none of the vaccinated patients experienced severe symptoms compared to 20.8% of unvaccinated patients.

NEUROLOGICAL SCIENCES (2023)

Article Multidisciplinary Sciences

The m6A reader YTHDC1 and the RNA helicase DDX5 control the production of rhabdomyosarcoma-enriched circRNAs

Dario Dattilo, Gaia Di Timoteo, Adriano Setti, Andrea Giuliani, Giovanna Peruzzi, Manuel Beltran Nebot, Alvaro Centron-Broco, Davide Mariani, Chiara Mozzetta, Irene Bozzoni

Summary: The study identifies m(6)A machinery and the RNA helicase DDX5 as factors responsible for the increase of a subset of circRNAs in RMS, providing protein and RNA candidates for the study of its tumorigenicity.

NATURE COMMUNICATIONS (2023)

Article Oncology

Distinguishable DNA methylation defines a cardiac-specific epigenetic clock

A. Mongelli, S. Panunzi, M. Nesta, M. Gottardi Zamperla, S. Atlante, V. Barbi, V. Mongiardini, F. Ferraro, S. De Martino, L. Cis, A. Re, S. Maltese, T. Bachetti, M. T. La Rovere, F. Martelli, M. Pesce, S. Nanni, M. Massetti, A. Pontecorvi, A. Farsetti, C. Gaetano

Summary: This study examines the emergence of epigenetic differences in the hearts of patients undergoing cardiac surgery and establishes an algorithm to determine how the pathophysiological condition can influence the biological age of the heart. The study reveals a similarity between chronological and biological age in the blood and heart, with telomere length being higher in the heart than in the blood. The cardiac-specific clock can discriminate between different types of cardiac surgery and is sensitive to cardiovascular risk factors.

CLINICAL EPIGENETICS (2023)

Article Microbiology

Modelling viral encephalitis caused by herpes simplex virus 1 infection in cerebral organoids

Agnieszka Rybak-Wolf, Emanuel Wyler, Tancredi Massimo Pentimalli, Ivano Legnini, Anna Oliveras Martinez, Petar Glazar, Anna Loewa, Seung Joon Kim, Benedikt B. Kaufer, Andrew Woehler, Markus Landthaler, Nikolaus Rajewsky

Summary: Modeling herpes simplex virus infection in brain organoids revealed that combined antiviral and anti-inflammatory treatment can prevent neuronal damage caused by viral infection. Despite antiviral treatment, herpes simplex encephalitis often results in neurological sequelae. The study used various techniques to characterize HSV-1 infection in human brain organoids and identified potential causal factors in neuronal damage and tissue perturbations. Combining anti-inflammatory drugs with antiviral treatment showed promise in preventing infection-related damages and improving therapeutic strategies.

NATURE MICROBIOLOGY (2023)

Article Biochemical Research Methods

Spatiotemporal, optogenetic control of gene expression in organoids

Ivano Legnini, Lisa Emmenegger, Alessandra Zappulo, Agnieszka Rybak-Wolf, Ricardo Wurmus, Anna Oliveras Martinez, Cledi Cerda Jara, Anastasiya Boltengagen, Tale Hessler, Guido Mastrobuoni, Stefan Kempa, Robert Zinzen, Andrew Woehler, Nikolaus Rajewsky

Summary: This study combines optogenetics and gene perturbation technologies to activate or knock down target genes in organoids with programmable spatiotemporal patterns. The research shows that local activation of specific signaling pathways is sufficient to generate organoids with stereotypical patterns and provides new insights into gene regulation in neurodevelopment. Thus, optogenetic perturbations in combination with spatial transcriptomics is a powerful technology for reprogramming and studying cell fates and tissue patterning in organoids.

NATURE METHODS (2023)

Article Cell Biology

circRNA-miRNA-mRNA Deregulated Network in Ischemic Heart Failure Patients

Alisia Made, Alessia Bibi, Jose Manuel Garcia-Manteiga, Anna Sofia Tascini, Santiago Nicolas Piella, Roman Tikhomirov, Christine Voellenkle, Carlo Gaetano, Przemyslaw Leszek, Serenella Castelvecchio, Lorenzo Menicanti, Fabio Martelli, Simona Greco

Summary: This study aims to explore the role of noncoding RNAs in cardiovascular diseases. The research found that circular RNAs can interact with microRNAs, regulating the expression of cardiovascular disease-related signaling pathways. Specifically, the study found that circBPTF is upregulated under hypoxia conditions and can regulate the function of endothelial cells by targeting miRNA targets such as HDAC9 and LRRC17.
Article Biochemistry & Molecular Biology

CircAFF1 Is a Circular RNA with a Role in Alveolar Rhabdomyosarcoma Cell Migration

Alvaro Centron-Broco, Francesca Rossi, Chiara Grelloni, Raffaele Garraffo, Dario Dattilo, Andrea Giuliani, Gaia Di Timoteo, Alessio Colantoni, Irene Bozzoni, Manuel Beltran Nebot

Summary: In this study, a circular RNA called circAFF1 was found to be overexpressed in alveolar rhabdomyosarcoma. Depletion of circAFF1 was shown to affect cell homeostasis and promote cell migration through the downregulation of genes involved in cell adhesion pathways. These findings highlight the potential of circAFF1 as a future therapeutic target for alveolar rhabdomyosarcoma.

BIOMEDICINES (2023)

Review Cardiac & Cardiovascular Systems

Integration of epigenetic regulatory mechanisms in heart failure

Miron Sopic, Emma L. Robinson, Costanza Emanueli, Prashant Srivastava, Claudio Angione, Carlo Gaetano, Gianluigi Condorelli, Fabio Martelli, Thierry Pedrazzini, Yvan Devaux

Summary: The field of epigenetics has gained attention in cardiovascular research due to its association with disease development. Multi-omics approaches that integrate different levels of disease regulation, such as DNA, histone, and RNA modifications, are essential for understanding complex diseases like cardiovascular diseases. This review focuses on discussing the role of epigenetic mechanisms in regulating gene expression and their interlinkage in the development of cardiac disease, particularly heart failure. The review also presents current methods and tools used for data integration and analysis, which can contribute to the discovery of novel therapeutic approaches and biomarkers for precision healthcare and improved clinical outcomes.

BASIC RESEARCH IN CARDIOLOGY (2023)

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