Ying Hu | Cancer Biology and Cancer Treatment | Best Researcher Award

Prof Ying Hu | Cancer Biology and Cancer Treatment | Best Researcher Award

Professor, Harbin Institute of technology, China

Prof. Ying Hu is a distinguished cancer biologist renowned for her groundbreaking research in tumor gene function, drug resistance, and cancer metastasis. With a PhD in Cancer Biology from University College London and an MPhil in Clinical Oncology from The Chinese University of Hong Kong, she has established herself as a leader in the field. Currently leading the tumor gene function study group at Harbin Institute of Technology, Prof. Hu focuses on uncovering novel therapeutic targets and mechanisms in cancer. Her work on oncogenes, long non-coding RNAs (lncRNAs), and the tumor microenvironment has been published in top-tier journals like Cancer Cell and PNAS. Prof. Hu is an active member of the Chinese Anti-Cancer Association and the Chinese Society for Cell Biology. Her research has significantly advanced our understanding of cancer biology, earning her recognition as a key contributor to the fight against cancer.

Professional Profile

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Scopus

Education 🎓

Prof. Ying Hu holds a PhD in Cancer Biology from University College London (2004-2009), where she specialized in tumor gene function. She earned her MPhil in Clinical Oncology from The Chinese University of Hong Kong (2002-2004) and an MS in Biochemistry and Molecular Biology from Fudan University (1999-2002). Her foundational education includes an MB in Chemical Analysis from Shandong Medical University (1994-1999). This diverse academic background has equipped her with a multidisciplinary approach to cancer research, combining molecular biology, clinical oncology, and biochemistry. Her education has been instrumental in shaping her innovative research strategies, enabling her to explore complex mechanisms of cancer progression and drug resistance.

Experience 💼

Prof. Ying Hu has over a decade of experience in cancer research. She currently leads the tumor gene function study group at Harbin Institute of Technology (2012-present), focusing on drug resistance and metastasis. Prior to this, she worked as a researcher at the University of Oxford (2009-2012), where she contributed to oncology research. Her expertise spans cellular and molecular biology, animal tumor models, and human sample analysis. Prof. Hu’s leadership has driven significant discoveries in cancer biology, including the role of lncRNAs and oncogenes in tumor progression. She is also an active member of professional organizations, including the Chinese Anti-Cancer Association and the Chinese Society for Cell Biology. Her extensive experience and leadership in cancer research have established her as a prominent figure in the field.

Awards and Honors 🏆

Prof. Ying Hu has received recognition for her outstanding contributions to cancer research. Her work has been featured in high-impact journals, with several papers highlighted as “Featured Articles” in Cancer Cell and PNAS. She has been an invited speaker at numerous international conferences, sharing her insights on cancer biology and drug resistance. Prof. Hu’s research on iASPP and lncRNAs has been widely cited, reflecting its significance in the field. She is a council member of the Chinese Society for Cell Biology (2019-present) and an active member of the Chinese Anti-Cancer Association. Her leadership and innovative research have earned her a reputation as a leading scientist in cancer biology. While specific awards are not listed, her consistent publication in top-tier journals and professional recognition underscore her achievements.

Research Focus 🔬

Prof. Ying Hu’s research focuses on understanding the mechanisms of drug resistance and cancer metastasis, the leading causes of cancer-related mortality. Her work explores the activation and function of oncogenes, such as the ASPP family proteins, and the roles of long non-coding RNAs (lncRNAs) in cancer progression. She investigates the interplay between tumor cells and the tumor microenvironment, using cellular and molecular strategies, animal models, and human samples. Key areas of her research include the regulation of apoptosis, ferroptosis, and DNA damage repair in cancer cells. Prof. Hu’s discoveries have identified novel therapeutic targets and provided insights into overcoming drug resistance. Her innovative approaches have advanced our understanding of cancer biology and opened new avenues for cancer treatment.

Publication Top Notes 📚

  1. iASPP is an antioxidative factor and drives cancer growth and drug resistance by competing with Nrf2 for Keap1 binding.
  2. SMURF2 predisposes cancer cells toward ferroptosis in GPX4-independent manners by promoting GSTP1 degradation.
  3. Long noncoding RNA HITT coordinates with RGS2 to inhibit PD-L1 translation in T cell immunity.
  4. ER-associated degradation ligase HRD1 links ER stress to DNA damage repair by modulating the activity of DNA-PKcs.
  5. iASPP suppresses Gp78-mediated TMCO1 degradation to maintain Ca2+ homeostasis and control tumor growth and drug resistance.
  6. Calcium homeostasis and cancer: insights from endoplasmic reticulum-centered organelle communications.
  7. AKAP1/PKA-mediated GRP75 phosphorylation at mitochondria-associated ER membranes protects cancer cells against ferroptosis.
  8. iASPP suppression mediates terminal UPR and improves BRAF-inhibitor sensitivity of colon cancers.
  9. A novel LncRNA HITT forms a regulatory loop with HIF-1α to modulate angiogenesis and tumor growth.
  10. A long noncoding RNA sensitizes genotoxic treatment by attenuating ATM activation and homologous recombination repair in cancers.
  11. LncRNA HITT inhibits metastasis by attenuating Rab5-mediated endocytosis in lung adenocarcinoma.
  12. iASPP is essential for HIF-1α stabilization to promote angiogenesis and glycolysis via attenuating VHL-mediated protein degradation.
  13. A lncRNA coordinates with Ezh2 to inhibit HIF-1α transcription and suppress cancer cell adaption to hypoxia.
  14. A previously identified apoptosis inhibitor iASPP confers resistance to chemotherapeutic drugs by suppressing senescence in cancer cells.
  15. Mitochondria-localized lncRNA HITT inhibits fusion by attenuating formation of mitofusin-2 homotypic or heterotypic complexes.
  16. lncRNA HITT Inhibits Lactate Production by Repressing PKM2 Oligomerization to Reduce Tumor Growth and Macrophage Polarization.
  17. HDAC1-induced epigenetic silencing of ASPP2 promotes cell motility, tumour growth, and drug resistance in renal cell carcinoma.
  18. Epigenetic silencing of ASPP1 confers 5-FU resistance in clear cell renal cell carcinoma by preventing p53 activation.
  19. EGR-1/ASPP1 inter-regulatory loop promotes apoptosis by inhibiting cyto-protective autophagy.
  20. Upregulation of MiR-205 under hypoxia promotes epithelial-mesenchymal transition by targeting ASPP2.
  21. A p53/CPEB2 negative feedback loop regulates renal cancer cell proliferation and migration.
  22. Nuclear iASPP determines cell fate by selectively inhibiting either p53 or NF-κB.
  23. Identification of lncRNA-Protein Interactions by CLIP and RNA Pull-Down Assays.
  24. Cell autonomous role of iASPP deficiency in causing cardiocutaneous disorders.
  25. iASPP prevents premature cellular senescence and is required for normal epithelial stratification.
  26. iASPP: A Novel Desmosome Regulator and its Deficiency Causes Arrhythmogenic Right Ventricular Cardiomyopathy.
  27. Restoring p53 function in human melanoma cells by inhibiting mdm2 and cyclinB1/cdk1 phosphorylated nuclear iASPP.

Conclusion 🏅

Prof. Ying Hu is a highly accomplished cancer biologist whose research has significantly advanced our understanding of drug resistance, cancer metastasis, and tumor gene function. With a strong educational background, extensive research experience, and numerous high-impact publications, she has established herself as a leader in the field. Her innovative approaches and discoveries have identified novel therapeutic targets and provided insights into overcoming cancer progression. Prof. Hu’s contributions to cancer biology make her a deserving candidate for the Best Researcher Award. Her work continues to inspire and pave the way for future breakthroughs in cancer treatment.

Mohamed Hassan | Tumor prevention and Therapy | Best Paper Award

Assist. Prof. Dr Mohamed Hassan | Tumor prevention and Therapy | Best Paper Award

Senior researcher, Tulane university school of medicine, United States

Mohamed Hassan is a distinguished researcher specializing in molecular oncology and translational medicine. He earned his Ph.D. from the University Hospital of Düsseldorf, Germany, focusing on Hepatitis C virus interactions with intracellular signaling. With extensive postdoctoral training in gastroenterology, pathology, and molecular tumor therapy, he has held academic positions in leading institutions across Germany, France, and the USA. His research spans cancer progression, drug resistance, and the tumor microenvironment, contributing to high-impact publications. Recognized globally for his scientific excellence, he has received prestigious awards, including the Italian Ministry of Health Award and the Japanese Society of Internal Medicine Award.

PROFESSIONAL PROFILE

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EDUCATION

  • Ph.D. (2001), University Hospital of Düsseldorf, Germany – Research on Hepatitis C virus core protein interference in liver cells.
  • M.Sc. (1996), University of Düsseldorf, Germany – Study on cDNA expression in malaria-immune mice.
  • B.Sc. (1983), Zagazig University & University of Düsseldorf, Germany.
  • Further Training: Teaching certification (University of Mississippi Medical Center, 2015), Clinical Research Associate (Germany, 2011), eLearning applications (University of Köln, 2008), and animal experimentation training (University of Düsseldorf, 2005).

EXPERIENCE

  • Senior Postdoctoral Fellow & PI – Institut National de la Santé et de la Recherche Médicale, University of Strasbourg (2007-2013).
  • Research Assistant Professor – Tulane University, USA (2016-2018); University of Strasbourg, France (2018-present).
  • Instructor – University of Mississippi Medical Center (2013-2016).
  • Postdoctoral Fellow – University Hospital of Düsseldorf (2001-2004).
  • Research Assistant – University Hospital of Düsseldorf (1996-2001); University of Düsseldorf (1992-1996).

AWARDS AND HONORS

🏅 2016 – Italian Ministry of Health Award for Research & Innovation.
🏅 2016 – Award of Excellence in Reviewing by Spandido Publications.
🏅 2011 – Japanese Society of Internal Medicine Outstanding Researcher Award.

RESEARCH FOCUS

🔬 Cancer Biology – Investigating tumor progression, metastasis, and resistance mechanisms.
🧬 Molecular Oncology – Targeting non-receptor tyrosine kinases in cancer therapy.
💊 Translational Medicine – Developing novel therapeutic strategies against cancer stem-like cells.
🦠 Immuno-oncology – Exploring immune checkpoint inhibitors and their effects.
🧑‍⚕️ Clinical Research – Bridging molecular insights with patient-centered treatments.

PUBLICATIONS

📄 Immune Checkpoint Inhibitor-Associated Cutaneous Adverse EventsInternational Journal of Molecular Sciences (2024)
📄 Non-Receptor Tyrosine Kinases in Tumor Progression and ResistanceCancers (2024)
📄 hTERT Epigenetics & Chemotherapy GuidanceInternational Journal of Molecular Sciences (2024)
📄 CD133-Dependent Activation in Melanoma ProgressionCells (2024)
📄 Mechanisms of Melanoma Progression & Treatment ResistanceCancers (2024)
📄 Tumor Microenvironment as a Therapeutic Target in MelanomaCancers (2023)
📄 Toll-like Receptors in Antimicrobial Protein ExpressionInternational Journal of Molecular Sciences (2023)
📄 Antimicrobial Proteins: Structure & Therapeutic PotentialPharmaceutics (2022)

CONCLUSION

Mohamed Hassan is a leading figure in molecular oncology, contributing groundbreaking research in cancer progression and therapy resistance. His work has been recognized internationally, and he continues to drive impactful discoveries in translational medicine and immuno-oncology. His commitment to scientific excellence is evident in his numerous high-impact publications and global collaborations. 🚀

Finn von Eyben | oncology | Best Researcher Award

Dr. Finn von Eyben | oncology | Best Researcher Award

chief, Center of Tobacco Control Reearch, Denmark.

Dr. Finn Edler von Eyben is a renowned specialist in internal medicine and oncology, with significant expertise across Denmark, Norway, and Sweden. He previously served as an administrative consultant at the Department of Internal Medicine, Queen Ingrid’s Hospital, Nuuk, Greenland. Dr. von Eyben is the author of multiple pivotal publications on testis cancer and prostate cancer, particularly in the field of radioligand therapy using PSMA. With a remarkable 12,914 reads and 2,788 citations of his work, he has made substantial contributions to oncological research. He has been invited to present at major international conferences, including those hosted at Innsbruck University, Austria. A prolific researcher, he also edited a theme issue on PSMA and prostate cancer for the International Journal of Molecular Sciences. His work spans over 164 publications, making him a leading figure in modern cancer research.

Profile:

Scopus

Education:

Dr. Finn Edler von Eyben completed his Doctor of Medicine at Southern Sweden in 1985, specializing in tumor markers for testicular cancer. Later, in 2005, he furthered his education at Southern Denmark, continuing his work on tumor markers for testis cancer. His educational foundation has been instrumental in shaping his deep understanding of cancer research, specifically in oncology and internal medicine. The combination of clinical and research-based education has allowed him to make lasting contributions to the medical field, focusing on advanced therapeutic techniques, radioligand therapy, and cancer biomarkers. Throughout his career, Dr. von Eyben has remained committed to advancing medical education through his research, aiming to provide a strong scientific basis for improving clinical outcomes in cancer care.

Experience:

Dr. Finn Edler von Eyben has built an extensive career in internal medicine and oncology across several countries, including Denmark, Norway, and Sweden. His administrative consultant role at the Department of Internal Medicine, Queen Ingrid’s Hospital in Nuuk, Greenland, showcased his leadership abilities in healthcare administration. With over three decades of clinical experience, Dr. von Eyben has been involved in groundbreaking cancer research and therapy, particularly concerning testis and prostate cancers. As a recognized authority, he has been a frequent speaker at international conferences, contributing his insights on PSMA and its role in prostate cancer treatment. His research focus on serum tumor markers and PSMA-based radioligand therapy has been widely influential, with his work being referenced globally. His expertise also extends to serving as the editor of journals and collaborating with fellow researchers, solidifying his position as a thought leader in oncology.

Awards and Honors:

Dr. Finn Edler von Eyben has earned widespread recognition for his outstanding contributions to oncology and internal medicine. His groundbreaking research on testis cancer and prostate cancer therapies has garnered over 2,788 citations, reflecting the high regard in which he is held by the scientific community. He was invited to serve as an editor for the International Journal of Molecular Sciences, where he contributed significantly to the PSMA and prostate cancer theme issue. His career has been marked by numerous invitations to deliver oral presentations at prestigious international conferences on nuclear medicine in oncology, including at Innsbruck University, Austria. Additionally, Dr. von Eyben’s research on radioligand therapy has positioned him at the forefront of the treatment of metastatic prostate cancer. While he has not publicly listed specific formal awards, the high citation index and frequent invitations to speak at conferences underscore the esteem he commands within the field.

Research Focus:

Dr. Finn Edler von Eyben is primarily focused on the treatment and diagnostic aspects of prostate cancer and testicular cancer. His research has greatly contributed to understanding tumor markers, especially in testis cancer, and has advanced the field of PSMA (Prostate-Specific Membrane Antigen)-based radioligand therapy. His notable work includes studies on 177Lu-PSMA-617 radioligand therapy for metastatic prostate cancer, which has revolutionized treatment strategies for castration-resistant prostate cancer. Dr. von Eyben has authored influential systematic reviews on the use of PSMA PET/CT scans in prostate cancer management, offering critical insights into optimal treatment regimens and early detection. Furthermore, his meta-analyses of choline PET/CT imaging for prostate cancer have solidified his role as a leader in nuclear medicine oncology. His work continues to shape clinical practices, focusing on personalized cancer treatments and improving patient outcomes through precision medicine.

Publication Titles:

  • 177Lu-PSMA-617 radioligand therapy for a patient with lymph node metastatic prostate cancer 🏥🔬
  • Third-line treatment and (177)Lu-PSMA radioligand therapy of metastatic castration-resistant prostate cancer: a systematic review 📚🧪
  • (177)Lu-PSMA radioligand therapy of predominant lymph node metastatic prostate cancer 🧬⚙️
  • Metastatic extent predicts survival as patients with metastatic castration-resistant prostate cancer are treated with (177)Lu-PSMA radioligand therapy ⏳🎯
  • (68)Ga-Labeled Prostate-specific Membrane Antigen Ligand Positron Emission Tomography/Computed Tomography for Prostate Cancer: A Systematic Review and Meta-analysis 📊🧠
  • Meta-analysis of (11)C-choline and (18)F-choline PET/CT for management of patients with prostate cancer 💡💊
  • Prostate-Specific Antigen as an Ultrasensitive Biomarker for Patients with Early Recurrent Prostate Cancer: How Low Shall We Go? A Systematic Review 🧪💉
  • Review on the Increasing Role for PSMA-Based Radioligand Therapy in Prostate Cancer 🏆📈

 

 

Chan-Yen Kuo | Tumor Immunology | Best Researcher Award

Assist. Prof. Dr Chan-Yen Kuo | Tumor Immunology | Best Researcher Award

Principal investigator, Tzu Chi University, Taiwan

Chan-Yen Kuo is a distinguished researcher and academic in the field of Cancer Biology, based in Taiwan. With a PhD in Life Science from Tunghai University, Dr. Kuo has made significant contributions to understanding cancer mechanisms, particularly in oral cancer, renal cell carcinoma, and hepatic stellate cell activation. Currently, he serves as an Adjunct Associate Professor at Jenteh Junior College of Medicine, Nursing and Management and as an Associate Investigator at Taipei Tzu Chi Hospital. His work integrates molecular biology, pharmacology, and traditional medicine to develop innovative therapeutic strategies. Dr. Kuo is also an active contributor to scientific literature, with numerous publications in high-impact journals.

Professional Profile

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Scopus

Strengths for the Award 🏆

  1. Prolific Research Output: Chan-Yen Kuo has an extensive publication record, with over 50 works in high-impact journals, demonstrating consistent contributions to the field of cancer biology and related areas. His research spans molecular mechanisms, therapeutic strategies, and the role of natural compounds in cancer treatment.
  2. Interdisciplinary Approach: Dr. Kuo’s work integrates molecular biology, pharmacology, and traditional medicine, showcasing a unique ability to bridge gaps between disciplines. His research on natural compounds like chrysophanol and their anti-cancer effects highlights innovative approaches to therapy.
  3. High-Impact Publications: Many of his papers are published in reputable journals such as Current Issues in Molecular BiologyBiomedicines, and Oxidative Medicine and Cellular Longevity, indicating the quality and relevance of his research.
  4. Focus on Translational Research: His work has practical implications for cancer diagnostics and treatment, particularly in understanding cancer stem cells, metastasis, and the role of inflammation and oxidative stress in tumorigenicity.
  5. Collaborative Efforts: Dr. Kuo frequently collaborates with other researchers, as evidenced by the numerous contributors listed in his publications. This demonstrates his ability to work in teams and contribute to larger scientific goals.
  6. Diverse Research Topics: His research covers a wide range of topics, including oral cancer, renal cell carcinoma, hepatic stellate cell activation, and even COVID-19 mortality predictors, showcasing versatility and depth.

Areas for Improvement 📉

  1. Citations and Impact Factor: While Dr. Kuo has a strong publication record, the citation counts and impact factors of some journals could be improved. Focusing on publishing in higher-impact journals could increase the visibility and influence of his work.
  2. International Recognition: Although his work is significant, greater international collaboration or participation in global conferences could enhance his global recognition and impact.
  3. Awards and Honors: There is limited information on specific awards or honors received by Dr. Kuo. Actively applying for prestigious awards or recognitions could further validate his contributions to the field.
  4. Clinical Trials: While his research is highly translational, there is limited evidence of direct involvement in clinical trials. Engaging in clinical research could bridge the gap between laboratory findings and real-world applications.
  5. Public Engagement: Increasing public engagement through science communication, interviews, or media appearances could help disseminate his research findings to a broader audience.

Education 🎓

Chan-Yen Kuo earned his PhD in Life Science from Tunghai University, Taichung, Taiwan, where he studied from 2004 to 2008. His doctoral research laid the foundation for his expertise in molecular biology and cancer research. During his academic journey, he developed a strong interest in the molecular mechanisms of cancer progression, particularly focusing on cell signaling pathways, oxidative stress, and inflammation. His educational background has equipped him with the skills to explore the intersection of traditional medicine and modern therapeutic approaches.

Experience 💼

Dr. Kuo has extensive experience in both academia and research. Since March 2022, he has been an Adjunct Associate Professor at Jenteh Junior College of Medicine, Nursing and Management, where he teaches and mentors students in medical technology. Additionally, since July 2021, he has served as an Associate Investigator at Taipei Tzu Chi Hospital, focusing on translational research in cancer biology. His previous roles include collaborations with various research institutions, where he investigated the role of bioactives, inflammation, and oxidative stress in cancer progression and therapy.

Awards and Honors 🏆

While specific awards and honors for Dr. Chan-Yen Kuo are not detailed in the provided information, his prolific publication record and leadership roles in cancer research indicate recognition within the scientific community. His work on topics such as EpCAM signaling, chrysophanol’s anti-cancer effects, and the role of inflammation in cancer has been widely cited, reflecting his impact on the field. Dr. Kuo’s contributions to high-impact journals and his involvement in cutting-edge research projects underscore his standing as a respected figure in cancer biology.

Research Focus 🔬

Dr. Kuo’s research focuses on understanding the molecular mechanisms of cancer progression and developing novel therapeutic strategies. His work spans several areas, including the role of cancer stem cells in metastasis, the impact of oxidative stress and inflammation on tumorigenicity, and the therapeutic potential of natural compounds like chrysophanol. He also explores the interplay between traditional medicine and modern pharmacology, aiming to identify bioactive compounds that can inhibit cancer cell growth, induce apoptosis, and modulate immune responses. His research has significant implications for improving cancer diagnostics and treatment.

Publication Top Notes 📚

  1. EpCAM Signaling in Oral Cancer Stem Cells: Implications for Metastasis, Tumorigenicity, and Therapeutic Strategies
  2. Molecular Biological Mechanisms of Action of Chrysophanol in Hepatic Stellate Cells Activated by Hepatic B Virus X Based on Network Pharmacology
  3. Diagnostics and Therapy for Malignant Tumors
  4. The Interplay between von Hippel–Lindau Tumor Suppressor Gene, Lon Protease, ROS Accumulation, and Inflammation in Clear Cell Renal Cell Carcinoma
  5. The Promising Potential of Caulerpa microphysa in Dermatology
  6. Tazarotene-induced Gene 1 Induces Melanoma Cell Death by Triggering Endoplasmic Reticulum Stress Response
  7. The Role of Bioactives in Inflammation
  8. Bioactives and Inflammation
  9. The COVIDTW study: Clinical predictors of COVID-19 mortality and a novel AI prognostic model using chest X-ray
  10. Pinostrobin and Tectochrysin Conquer Multidrug-Resistant Cancer Cells via Inhibiting P-Glycoprotein ATPase
  11. The von Hippel-Lindau Tumor Suppressor Gene Mutations Modulate Lipocalin-2 Expression in Ferroptotic-Inflammatory Pathways
  12. Pharmacological Interventions for Excessive Daytime Sleepiness in Adults with Narcolepsy: A Systematic Review and Network Meta-Analysis
  13. Coumarin Derivatives Inhibit ADP-Induced Platelet Activation and Aggregation
  14. Chrysophanol Suppresses Cell Growth via mTOR/PPAR-α Regulation and ROS Accumulation in Cultured Human Tongue Squamous Carcinoma SAS Cells
  15. Combined Acupoints for the Treatment of Patients with Obesity: An Association Rule Analysis
  16. Wild Bitter Melon Extract Abrogates Hypoxia-Induced Cell Death via the Regulation of Ferroptosis, ER Stress, and Apoptosis in Microglial BV2 Cells
  17. An Association Rule Analysis of Combined Acupoints for the Treatment of Patients with Dry Eye Disease
  18. An Association Rule Analysis of the Acupressure Effect on Sleep Quality
  19. Nephroprotective Role of Chrysophanol in Hypoxia/Reoxygenation-Induced Renal Cell Damage via Apoptosis, ER Stress, and Ferroptosis
  20. Poria cocos Regulates Cell Migration and Actin Filament Aggregation in B35 and C6 Cells by Modulating the RhoA, CDC42, and Rho Signaling Pathways
  21. Tournefortia sarmentosa Inhibits the Hydrogen Peroxide-Induced Death of H9c2 Cardiomyocytes
  22. Anti-Cancer Effects of Zotarolimus Combined with 5-Fluorouracil Treatment in HCT-116 Colorectal Cancer-Bearing BALB/c Nude Mice
  23. Role of the Inflammatory Response of RAW 264.7 Cells in the Metastasis of Novel Cancer Stem-Like Cells
  24. Wild Bitter Melon Extract Regulates LPS-Induced Hepatic Stellate Cell Activation, Inflammation, Endoplasmic Reticulum Stress, and Ferroptosis
  25. Safflower Extract Inhibits ADP-Induced Human Platelet Aggregation
  26. Interleukin-6 and Interleukin-8 Regulate STAT3 Activation Migration/Invasion and EMT in Chrysophanol-Treated Oral Cancer Cell Lines
  27. The Anti-Cancer Effects of a Zotarolimus and 5-Fluorouracil Combination Treatment on A549 Cell-Derived Tumors in BALB/c Nude Mice
  28. An Apriori Algorithm-Based Association Rule Analysis to Identify Acupoint Combinations for Treating Diabetic Gastroparesis
  29. Poor Work Efficiency is Associated with Poor Exercise Capacity and Health-Related Quality of Life in Patients with Chronic Obstructive Pulmonary Disease
  30. Loss of Function of von Hippel‐Lindau Trigger Lipocalin 2‐Dependent Inflammatory Responses in Cultured and Primary Renal Tubular Cells
  31. Establishment of an Immunocompetent Metastasis Rat Model with Hepatocyte Cancer Stem Cells
  32. Dietary Patterns and the Risk of Prediabetes in Taiwan: A Cross-Sectional Study
  33. A Meta-Analysis of Comparing Intermittent Epidural Boluses and Continuous Epidural Infusion for Labor Analgesia
  34. Wild Bitter Melon Exerts Anti-Inflammatory Effects by Upregulating Injury-Attenuated CISD2 Expression following Spinal Cord Injury
  35. An Apriori Algorithm‐Based Association Rule Analysis to Identify Herb Combinations for Treating Uremic Pruritus Using Chinese Herbal Bath Therapy
  36. Chrysophanol Prevents Lipopolysaccharide‐Induced Hepatic Stellate Cell Activation by Upregulating Apoptosis, Oxidative Stress, and the Unfolded Protein Response
  37. Chrysophanol Regulates Cell Death, Metastasis, and Reactive Oxygen Species Production in Oral Cancer Cell Lines
  38. Combination of Acupoints in Treating Patients with Chronic Obstructive Pulmonary Disease: An Apriori Algorithm‐Based Association Rule Analysis
  39. Neuronal CISD2 plays a minor anti-inflammatory role in LPS-stimulated neuron-like SH-SY5Y cells
  40. Oridonin Attenuates Lipopolysaccharide‐Induced ROS Accumulation and Inflammation in HK‐2 Cells
  41. Role of Chrysophanol in Epithelial‐Mesenchymal Transition in Oral Cancer Cell Lines via a Wnt‐3‐Dependent Pathway
  42. Danshensu Attenuates Hypoxia-Induced Reactive Oxygen Species Production and Inducible Nitric Oxide Synthase Expression in RAW 264.7 Cells
  43. Prevotella denticola septic embolic cerebral infarction after difficult lower wisdom tooth extraction
  44. Tazarotene-Induced Gene 1 (TIG1) Interacts with Serine Protease Inhibitor Kazal-Type 2 (SPINK2) to Inhibit Cellular Invasion of Testicular Carcinoma Cells
  45. Apoptotic effects of hsian‐tsao (Mesona procumbens Hemsley) on hepatic stellate cells mediated by reactive oxygen species and ERK, JNK, and caspase‐3 pathways
  46. Endothelial-cell inflammation and damage by reactive oxygen species are prevented by propofol via ABCA1-mediated cholesterol efflux
  47. The protective effect of simvastatin against ultraviolet B-induced corneal endothelial cell death
  48. UVB promotes the initiation of uveitic inflammatory injury in vivo and is attenuated by UV-blocking protection
  49. VHL Inactivation in Precancerous Kidney Cells Induces an Inflammatory Response via ER Stress–Activated IRE1α Signaling

Conclusion 🎯

Chan-Yen Kuo is a highly accomplished researcher with a strong track record in cancer biology, particularly in understanding the molecular mechanisms of cancer progression and developing innovative therapeutic strategies. His interdisciplinary approach, high-quality publications, and collaborative efforts make him a strong candidate for the Best Researcher Award.

However, to further strengthen his candidacy, Dr. Kuo could focus on increasing the impact factor of his publications, seeking international recognition, and engaging in clinical trials or public outreach. Overall, his contributions to the field are significant, and with a few strategic improvements, he could solidify his position as a leading researcher in cancer biology.