Rut Valdor | Cell Therapy In Neurology | Best Researcher Award

Ms. Rut Valdor | Cell Therapy In Neurology | Best Researcher Award

Researcher PhD, University of Murcia, Spain

Dr. Rut Valdor Alonso is a distinguished biomedical scientist and Ramón y Cajal (R3-accredited) Researcher at the University of Murcia, Spain. Her pioneering work focuses on chaperone-mediated autophagy (CMA) and its implications in glioblastoma progression, pericyte biology, and immune modulation. With over 17 high-impact publications, three patents, and significant leadership roles in international research networks, she stands as a leading voice in translational cancer research and molecular immunology. Her work continues to influence the future of advanced therapies in neuro-oncology and regenerative medicine.

Professional Profile

Scopus Profile

ORCID

Education

Dr. Valdor earned her Ph.D. in Biology from the University of Murcia in 2008, with a strong focus on cellular and molecular biology. Following her doctoral training, she received the prestigious Seneca Foundation fellowship and began her postdoctoral work at the Virgen de la Arrixaca Hospital’s Experimental Surgery Unit. She then joined the Albert Einstein College of Medicine in New York (2009–2014) as a postdoctoral fellow through an NIH-funded program, where she investigated the role of CMA in aging and T-cell activation. These experiences laid the foundation for her interdisciplinary approach to immune regulation and cancer biology.

Experience

Throughout her career, Dr. Valdor has held pivotal research positions across respected institutions in Spain and the United States. She started her postdoctoral career in Spain at the Fundación para la Formación e Investigación Sanitarias (FFIS) and later at the Department of Anatomy and Psychobiology at the University of Murcia. From 2017 to 2020, she served as a Principal Investigator (PI) under the competitive JIN-MINECO program, where she directed studies on pericytes and immune function in glioblastoma. In 2021, she was awarded the Ramón y Cajal fellowship, a highly competitive national program, which enabled her to launch a dedicated line of research on therapeutic modulation of CMA at the University of Murcia. In addition to her research, Dr. Valdor is an active academic mentor, having supervised numerous postdoctoral fellows, doctoral candidates, and undergraduate students, playing a crucial role in shaping the next generation of scientists.

Research Focus

Dr. Valdor’s research centers on unraveling the cellular mechanisms that govern immune responses, tumor progression, and tissue repair, with particular emphasis on chaperone-mediated autophagy (CMA). She has uncovered how glioblastoma hijacks CMA in pericytes to promote immune suppression, paving the way for novel therapeutic interventions. Her research has led to the development of genetically modified pericytes as potential anti-tumoral agents and is backed by several national and European-funded projects. Dr. Valdor’s cutting-edge work offers promising avenues for treating aggressive brain tumors and chronic inflammatory conditions through modulation of CMA pathways.

Awards & Honors

Dr. Valdor’s outstanding achievements have been widely recognized through numerous national and international awards and fellowships. Early in her career, she was honored with the Keystone Symposium Postdoctoral Award in British Columbia and the Daniel Shields Travel Award at Albert Einstein College of Medicine. Her excellence continued with a postdoctoral fellowship from the NIH and further funding through the Seneca Foundation. She received the MINECO-JIN fellowship to lead her own research group and was later selected for the prestigious Ramón y Cajal program, a testament to her leadership in Spanish biomedical research. Her presentations have received accolades, including Best Communication Prizes at the IMIB-Arrixaca Research Conferences in both 2018 and 2019. In addition to academic distinctions, she has also received support from Fundación La Caixa and Fundación Seneca to advance her translational research. Her appointment in 2025 as a “Profesor Titular” (ANECA-accredited) and her election as Co-Chair of the Women in Autophagy (WIA) Scientific Committee further reflect her professional excellence and commitment to promoting gender equity in science.

Publication Top Notes

Expression of Lumican and Osteopontin in Perivascular Areas of the Glioblastoma Peritumoral Niche and Its Value for Prognosis

Journal: International Journal of Molecular Sciences
Authors: María Dolores Salinas, Pablo Rodriguez, Gonzalo Rubio, Rut Valdor
Summary: This study investigates the expression patterns of Lumican and Osteopontin, two extracellular matrix proteins, within perivascular areas of the glioblastoma peritumoral niche. The research reveals that high expression levels of these proteins correlate with specific prognostic outcomes, potentially serving as biomarkers for tumor aggressiveness. Dr. Valdor contributed to the molecular characterization and immunohistological analysis, offering insights into the tumor microenvironment’s role in glioblastoma progression and recurrence.

The Role of Chaperone-Mediated Autophagy in Tissue Homeostasis and Disease Pathogenesis

Journal: Biomedicines
Authors: Rut Valdor, Marta Martinez-Vicente
Summary: This comprehensive review discusses the pivotal role of chaperone-mediated autophagy (CMA) in maintaining tissue homeostasis and regulating pathological processes, particularly in neurodegenerative diseases, cancer, and immune dysfunctions. Dr. Valdor elaborates on how dysregulation of CMA contributes to disease mechanisms and highlights its therapeutic potential as a targetable pathway. The article integrates findings across multiple models to emphasize CMA’s physiological relevance.

Pericytes, a Cell Type Contributing to Autoimmunity and Immune Tolerance

Book Chapter: Translational Neuroimmunology, Volume 7
Authors: Maria Botía-Sánchez, Maria Luisa Molina, Pedro Aparicio, Rut Valdor
Summary: This chapter provides an in-depth examination of pericytes as immunomodulatory cells involved in the regulation of both autoimmunity and immune tolerance. The authors detail how pericytes influence immune cell trafficking, cytokine release, and local immune responses in the central nervous system. Dr. Valdor contributes her expertise on chaperone-mediated autophagy in pericytes, emphasizing its relevance in neuroinflammation and autoimmunity. The chapter positions pericytes as a promising cellular target for immune-based therapies.

Chaperone-Mediated Autophagy in Pericytes: A Key Target for the Development of New Treatments against Glioblastoma Progression

Journal: International Journal of Molecular Sciences
Authors: María Dolores Salinas, Rut Valdor
Summary: This article identifies chaperone-mediated autophagy (CMA) in pericytes as a critical factor in glioblastoma development. The study demonstrates that modulating CMA alters the immunosuppressive behavior of pericytes within the tumor microenvironment. Targeting CMA can enhance the anti-tumoral functions of pericytes, suggesting a novel therapeutic avenue for glioblastoma treatment. Dr. Valdor served as corresponding author, underscoring her leadership in the field.

Chaperone-Mediated Autophagy Ablation in Pericytes Reveals New Glioblastoma Prognostic Markers and Efficient Treatment Against Tumor Progression

Journal: Frontiers in Cell and Developmental Biology
Authors: Molina ML, García-Bernal D, Salinas MD, Rubio G, Aparicio P, Moraleda JM, Martínez S, Valdor R
Summary: This experimental study provides compelling evidence that genetic ablation of CMA in pericytes significantly impairs glioblastoma progression. The absence of CMA not only reduces tumor-supportive functions but also unmasks prognostic biomarkers linked to patient outcomes. The findings support the development of CMA-targeted peptide therapies, and Dr. Valdor’s contribution as senior researcher and co-author reflects her active role in designing and interpreting the study’s therapeutic implications.

Conclusion

Dr. Rut Valdor Alonso is an innovative and dynamic researcher whose work at the intersection of autophagy, immunology, and cancer therapy holds significant promise for the future of personalized medicine. Through her trailblazing research on pericytes and glioblastoma, her international collaborations, and her mentorship of emerging scientists, she has made substantial contributions to both science and society. Her remarkable achievements make her an exemplary nominee for this prestigious award.

Shunbin Ning | Immunotherapy | Best Researcher Award

Dr. Shunbin Ning | Immunotherapy | Best Researcher Award

Professor, East Tennessee State University, United States

Professor Shunbin Ning is a renowned expert in viral oncology and immunology, with a passion for uncovering the intricate mechanisms of chronic viral infections and immune deregulation. 🌐🔍 His groundbreaking work explores how viruses like EBV and HTLV1 disrupt immune checkpoints, DNA damage response, and metabolic pathways to establish latency and drive cancer progression. 🧬🛡️ As a Professor at ETSU’s Quillen College of Medicine and a Scientist at the Mountain Home VA Medical Center, he has led NIH- and DoD-funded research projects focused on long noncoding RNAs, selective autophagy, and oncogenic IRFs. 📚🧪 With over 100 publications and editorial roles across several scientific journals, he is a respected voice in the field. 📖🧠 His mentorship and leadership have significantly contributed to the advancement of viral immunopathology and novel immunotherapeutic strategies. 🌟👨‍🔬

💠Professional Profile

Google Scholar

🎓 Education 

Professor Ning began his academic journey at Wuhan University, China, earning his B.S. in Cell Biology in July 1996. 🎓🔬 He further pursued a Ph.D. in Cell Biology and Genetics at the same institution, which he completed in December 2001. 🧬📘 Driven by a passion for research, he moved to the United States for postdoctoral training in Viral Oncology and Immunology at UNC Chapel Hill, completing it in March 2007. 🇺🇸🧫 His academic path continued with roles as Research Associate and later as Research Assistant Professor at UNC, where he deepened his expertise in host-pathogen interactions, chronic infections, and immune system regulation. 🧠🧪 His education set a strong foundation for a prolific research career at the intersection of virology, immunology, and cancer biology. 🌍📚

💼 Experience 

With over two decades of academic and research excellence, Professor Ning has held significant positions in top institutions. 🏛️🧑‍🔬 Since 2024, he has served as Professor in Internal Medicine at ETSU’s Quillen College of Medicine and a Scientist at the Department of Veterans Affairs in Tennessee. 🇺🇸⚕️ Previously, he held roles as Associate and Assistant Professor at ETSU and the University of Miami’s Sylvester Cancer Center. 🧪📍 He also contributes as Affiliate Assistant Professor at the University of Central Florida. 🧑‍🏫 His leadership extends into the VA system as a WOC employee, reflecting his dedication to veteran health. 🪖❤️ His academic journey spans teaching, mentorship, and pioneering research in viral oncology and immunopathogenesis, making him a pivotal figure in translational medicine. 🔄🎓

🧪 Research Focus 

Professor Ning’s research is anchored in viral immunology and oncogenesis, particularly chronic infections like EBV and HTLV1. 🧫🧬 He explores how these viruses manipulate host immunity via DNA damage response (DDR), autophagy, immune checkpoints, and non-coding RNAs. 🔍🧠 His studies decode how these mechanisms foster viral latency, immune evasion, and cancer transformation. 🦠💥 Key areas include oxidative stress, interferon regulation, and ubiquitin-mediated signaling, revealing novel insights into inflammaging and tumor microenvironments. 🌡️🧪 His translational work identifies new immunotherapeutic targets for virus-associated diseases, especially in hematological malignancies. 🎯🧬 He also pioneers research into lncRNAs’ role in lymphoma development and IRF4 regulation in oncogenesis. 📊🧬 Through innovative methodologies, including phosphoproteomics and transcriptomics, he advances understanding of virus-host interactions, helping bridge molecular mechanisms with therapeutic strategies. 🧪💡

🏅 Awards and Honors 

Professor Ning’s excellence has been recognized through numerous prestigious awards. 🏆🎓 He is a two-time awardee of the American Society of Hematology (ASH), receiving both a Scholarship (2012) and Bridge Grant (2020) for his impactful research. 🔬💰 His accolades include the Leukemia Research Foundation Award (2010), Florida Department of Health New Investigator Award (2010), and an International Professorship Award from the ASM (2009). 🌍📜 Early in his career, he earned the Excellent PhD Thesis Award from both Wuhan University (2003) and China’s Ministry of Education (2005), as well as being named a top graduate student (2002). 🧑‍🎓🌟 His commitment to mentoring and service has also been honored by ASM for outstanding contributions to online mentoring and international programs. 💻🤝 These accolades reflect his scientific impact and dedication to global research advancement. 🌐💡

📘 Publications Top Notes

Guidelines for the Use and Interpretation of Assays for Monitoring Autophagy (4th Edition)

Authors: D.J. Klionsky, A.K. Abdel-Aziz, S. Abdelfatah, M. Abdellatif, A. Abdoli, S. Abel, et al. (including S. Ning)
Journal: Autophagy, Volume 17, Issue 1, Pages 1–382 (2021)
Summary:
This comprehensive and collaborative work offers updated guidelines for monitoring autophagy in both in vivo and in vitro systems. 🧪📚 With contributions from hundreds of experts, including Dr. Ning, it covers key assays, markers, and interpretations critical for studying autophagy accurately. 🔍🧫 These standardized protocols ensure reproducibility across labs and support the effective application of autophagy-related research in fields such as cancer, neurodegeneration, and infectious diseases. 🌍🔬 An essential resource, this publication has become the gold standard for autophagy research worldwide. 🌟

IRF7: Activation, Regulation, Modification and Function

Authors: S. Ning, J.S. Pagano, G.N. Barber
Journal: Genes & Immunity, Volume 12, Issue 6, Pages 399–414 (2011)
Summary:
This review article highlights the central role of IRF7, a key transcription factor in antiviral immunity. 🛡️🧬 Dr. Ning and colleagues discuss its activation pathways, post-translational modifications, and regulatory networks, especially in the context of type I interferon production. ⚙️📊 The paper emphasizes IRF7’s importance in immune responses to viral infections like EBV, and its manipulation by viruses to evade immunity. 🦠⚠️ A valuable resource for understanding host-virus interactions and the molecular immunology of viral pathogenesis. 🧫📖

Salt Stress Induces Programmed Cell Death in Prokaryotic Organism Anabaena

Authors: S.B. Ning, H.L. Guo, L. Wang, Y.C. Song
Journal: Journal of Applied Microbiology, Volume 93, Issue 1, Pages 15–28 (2002)
Summary:
This early study by Dr. Ning explores how salt stress triggers programmed cell death (PCD) in the cyanobacterium Anabaena. 🧂🔬 The research identifies morphological and molecular changes indicative of apoptosis-like pathways, suggesting that even prokaryotes possess regulated death mechanisms under stress. ⚡🧫 This foundational work contributes to the broader understanding of cell death evolution and microbial stress responses. 🌱🧠

TRAF6 and the Three C-terminal Lysine Sites on IRF7 Are Required for Its Ubiquitination-mediated Activation by the Tumor Necrosis Factor Receptor Family Member Latent Membrane Protein 1

Authors: S. Ning, A.D. Campos, B.G. Darnay, G.L. Bentz, J.S. Pagano
Journal: Molecular and Cellular Biology, Volume 28, Issue 20, Pages 6536–6546 (2008)
Summary:
This experimental study details how Epstein-Barr virus (EBV) protein LMP1 activates IRF7 via TRAF6-dependent ubiquitination. 🧬🔁 Dr. Ning and co-authors show that three specific lysine residues on IRF7 are essential for its activation, linking viral oncogenesis with host immune signaling. 🧪⚙️ This discovery sheds light on viral immune evasion and provides targets for antiviral strategies. 🦠💡

Interferon Regulatory Factor 7 Is Negatively Regulated by the Epstein-Barr Virus Immediate-Early Gene, BZLF-1

Authors: A.M. Hahn, L.E. Huye, S. Ning, J. Webster-Cyriaque, J.S. Pagano
Journal: Journal of Virology, Volume 79, Issue 15, Pages 10040–10052 (2005)
Summary:
This research reveals that EBV gene BZLF-1 suppresses the expression and function of IRF7, undermining the host’s antiviral interferon response. 🚫🧬 Dr. Ning contributed to showing how BZLF-1 impairs IRF7-mediated signaling, helping the virus establish latency and avoid immune detection. 🧫👁️ This work provides crucial insight into the immune evasion tactics of herpesviruses and their impact on host immunity. 🧠🦠

Professor Shunbin Ning stands at the forefront of viral immunology and cancer biology, contributing transformative insights into virus-host interactions. 🧬🌍 His pioneering research on EBV, immune regulation, and non-coding RNAs bridges fundamental biology with therapeutic potential. 🎯🧠 His dedication to mentorship, global collaboration, and editorial leadership enriches the scientific ecosystem. 🌱🌐 Through over 100 publications, continuous NIH/DoD-funded projects, and service on international boards and review panels, Professor Ning continues to inspire innovation and excellence in biomedical science. 📚🏅 His work not only deepens our understanding of chronic viral infections but also charts new paths toward immunotherapeutic breakthroughs. 💡💊 A true leader and visionary in his field, he exemplifies the synergy of scientific rigor and clinical relevance. 🧑‍🔬❤️