Skip to main content
Biomolecules & Therapeutics logoLink to Biomolecules & Therapeutics
. 2024 Dec 31;33(1):1–4. doi: 10.4062/biomolther.2024.007

Emerging and Promising Keywords in Biomolecules and Therapeutics for 21st Century Diseases

Hyun-Jeong Ko 1, Chang Hoon Lee 2,*
PMCID: PMC11704395  PMID: 39725476

Abstract

Recent technological advancements and environmental changes are leading to an increase in various diseases such as obesity, fibrosis, metabolic disorders, and degenerative diseases associated with aging. Additionally, micro- and nanoplastics are emerging as as potential contributors to many of these conditions, posing a serious threat to human health. This special issue aims to explore new directions and opportunities for future drug development through recent review articles published in the issue, focusing on these key medical topics.

Keywords: Obesity, Fibrosis, Metabolic disorders, Degenerative diseases, Micro- and nonoplastics

INTRODUCTION

In recent years, technological advancements and the emergence of new environmental risk factors have led to an increase in global disease occurrences, bringing forth new keywords that require our attention. We aim to review research trends by compiling seven key papers spanning diverse topics, including obesity, fibrosis, metabolic and degenerative diseases, cancer and nerve connectivity, microplastics, the gut microbiome, natural compounds, and stem cell therapies. Through this comprehensive review, we aim to extract integrative ideas from these different keywords and generate insights for future advancements in biomedical research and innovative drug development.

KEYWORDS IN BIOMOLECULES AND THERAPEUTICS FOR 21ST CENTURY DISEASES

Obesity: GLP-1 agonist & beyond

The first paper focuses on obesity, for which drug development research is actively ongoing by global and domestic pharmaceutical companies (Special issue 1) (Kim and Kim, 2025). As is well known, the increasing trend of obesity triggers numerous complications, including allergies, psoriasis, type 2 diabetes, cardiovascular diseases, and specific cancers, necessitating a multifaceted approach to treatment. The Biomolecules & Therapeutics journal has also seen an increase in obesity-related papers in recent years (Hwang et al., 2020; Piao et al., 2022; Cha et al., 2023; Han et al., 2023b). While existing anti-obesity drugs have achieved some success, new drug developments that go beyond simply reducing energy intake show promising potential for achieving greater weight loss and improving obesity-related complications (Müller et al., 2022; Novikoff et al., 2024). We believe that a combination of innovative drug therapies and lifestyle changes can provide new hope for addressing obesity, a global health challenge.

Metabolic dysfunction-associated steatotic liver disease and hepatic fibrosis: AMPK inhibitor

Moreover, as metabolic dysfunction-associated liver disease (MASLD) and other chronic liver diseases increase, the development of new strategies for liver protection and disease progression prevention has become crucial (Raza et al., 2024). The second paper specifically addresses these new strategies (special issue 2) (An et al., 2025). AMP-activated protein kinase (AMPK) activators have already emerged as promising candidates for various diseases due to their broad regulatory effects on major metabolic and inflammatory pathways (Jeong et al., 2016; Rho et al., 2021; Penugurti et al., 2024; Pokhrel et al., 2024). By modulating lipid metabolism, insulin resistance, and inflammatory cascades, AMPK activators show potential to halt or reverse the progression of MASLD, liver fibrosis, and even hepatocellular carcinoma.

Kidney Disease: natural products

The global burden of increasing kidney diseases, particularly diabetic kidney disease (DKD) as a complication of diabetes mellitus, necessitates a paradigm shift in treatment strategies (Wada and Makino, 2016; Natesan and Kim, 2021). Traditionally, treatment for diseases like DKD has focused on symptom management and slowing disease progression. However, recent studies exploring the role of natural compounds and combination therapies have emphasized their potential not only to prevent but also to reverse kidney damage (Sun et al., 2022; Jung et al., 2023; Ahn and Park, 2024; Choi et al., 2024). Bioactive substances, such as polyphenols found in various foods, have emerged as promising candidates for preventing diabetic nephropathy and mitigating oxidative stress and inflammation, which contribute to kidney dysfunction (Special issue 3) (Natesan and Kim, 2025). As these compounds are further scientifically investigated, the therapeutic potential of natural substances in kidney disease treatment could offer a new complementary approach to existing pharmacological interventions.

Neurodegenerative disease: probiotics

Recently, many researchers have significantly increased their focus on brain and neurological disorders, as well as the development of treatments for these conditions (Han et al., 2023; Creekmore et al., 2024; Kim, 2024; Lefevre-Arbogast et al., 2024; Nixon and Rubinsztein, 2024; Yajing et al., 2024). The occurrence of neurodegenerative diseases (NDDs), such as Alzheimer’s and Parkinson’s disease, further emphasizes the complexity of modern healthcare (Coukos and Krainc, 2024; Jackson et al., 2024; Korczyn and Grinberg, 2024; Morris et al., 2024). These diseases are characterized by progressive neurodegeneration and pose substantial challenges to global health systems. In response to these challenges, the gut microbiome has emerged as a novel therapeutic approach (Kwon et al., 2024; Lee et al., 2024; Seo and Holtzmann, 2024). Research into the gut-brain axis and the role of microorganisms in neurodegeneration has opened new pathways for understanding how external factors influence brain health (Special issue 4) (Kim et al., 2025). In particular, probiotics have garnered attention for their potential to modulate neurodegenerative processes and provide therapeutic benefits. Specific probiotic strains, such as Lactobacillus plantarum, Bifidobacterium breve, and Lactobacillus rhamnosus, may offer novel approaches to managing these debilitating diseases, providing potential benefits that go beyond symptom management.

Cancer-nerve intersection: DX2

Interest in brain and neuroscience is rapidly expandingwithin the field of cancer (Hutchings et al., 2020; Lee et al., 2020; Winkler et al., 2023; Lyu et al., 2024; Poh, 2024). Specifically, research that previously focused on the microenvironment in cancer is now also drawing attention to the neural microenvironment, which contributes to immune suppression (Mancusi and Monje, 2023; Xu et al., 2024). In addition to the numerous research trends studying how nerves interact within the cancer microenvironment, recent approaches have increasingly emphasized applying cancer research findings to neurodegenerative brain diseases. This research trend is particularly addressed in this special issue (Special issue 5) (Baek, 2025). Survival genes like DX2 play crucial roles in both cancer and neurodegeneration. DX2, a spliced variant of AIMP2 with deletion of exon 2, is overexpressed in various cancers and regulates cell death pathways, presenting a potential target for anti-cancer therapies. Interestingly, genes traditionally considered oncogenes, such as AKT and XBP1, are now being studied for their neuroprotective effects in neurodegenerative diseases, bringing about strategic changes in therapeutic applications.

Osteoarthritis: stem cell

Following the potential of treating neurodegenerative brain diseases using microbiome, research on treating degenerative diseases using stem cells and their derived exosomes continues steadily (Ni et al., 2020; Ehioghae et al., 2024; Kim et al., 2024; Li et al., 2024; Tian et al., 2024). In the musculoskeletal health field, osteoarthritis remains a major cause of disability, with current treatments primarily focused on symptom management. However, stem cell therapy for knee joint cartilage regeneration is considered a promising alternative (Special issue 6) (Lee et al., 2025). Stem cell injections offer the potential to provide long-term relief for osteoarthritis patients by promoting cartilage regeneration and reducing pain and inflammation, thereby opening a path to avoid more invasive procedures like joint replacement surgery. We anticipate that stem cell-based therapies will expand to address a wider range of degenerative diseases.

Micro- and naonplastics: new emerging etiology

One of the most serious consequences of widespread plastic use is environmental pollution by microplastics (MPs) and nanoplastics (NPs), along with the diseases they may cause (de Oliveira et al., 2024; Goswami et al., 2024; Liao et al., 2024; Liu et al., 2024; Sun et al., 2024; Zhao et al., 2024; Zheng et al., 2024). These small plastic particles, created as plastic products break down, have been found in marine organisms, wildlife, and even in human bodies. However, despite their widespread presence, recent reports have highlighted their potential role as disease agents, yet our understanding of their immunological impacts remains limited (Special issue 7) (Dan et al., 2025). Preliminary research suggests these particles can interact with the immune system in complex ways, potentially exerting differential effects depending on their material, size, and shape. As global efforts to reduce plastic pollution intensify, it is critically important to comprehensively understand the impact of MPs and NPs on immune health, especially given their potential to exacerbate or trigger diseases.

CONCLUSION

In this special issue, we have published review articles covering keywords related to both recently emerging and long-standing yet unresolved diseases. Through the exploration of these individual keywords and new efforts understand them comprehensively, we believe we can continue to make progress towards innovation in addressing 21st-century diseases.

REFERENCES

  1. Ahn Y., Park J. H. Novel potential therapeutic targets in autosomal dominant polycystic kidney disease from the perspective of cell polarity and fibrosis. Biomol. Ther. (Seoul) 2024;32:291–300. doi: 10.4062/biomolther.2023.207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. An H., Jang Y., Choi J., Hur J., Kim S. J., Kwon Y. New insights into AMPK, as a potential therapeutic target in metabolic dysfunction-associated steatotic liver disease and hepatic fibrosis. Biomol. Ther. (Seoul) 2025;33:18–38. doi: 10.4062/biomolther.2024.188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Baek K. The dual role of survival genes in neurons and cancer cells: a strategic clinical application of DX2 in neurodegenerative diseases and cancer. Biomol. Ther. (Seoul) 2025;33:75–85. doi: 10.4062/biomolther.2024.138. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cha Y. J., Chang I. A., Jin E.-H., Song J. H., Hong J. H., Jung J.-G., Sunwoo J. Association between LEPR genotype and gut microbiome in healthy non-obese Korean adults. Biomol. Ther. (Seoul) 2023;32:146–153. doi: 10.4062/biomolther.2023.116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Choi H. G., Park S. Y., Bae S. H., Chang S.-Y., Kim S. H. Loganin ameliorates acute kidney injury and restores tofacitinib metabolism in rats: implications for renal protection and drug interaction. Biomol. Ther. (Seoul) 2024;32:601–610. doi: 10.4062/biomolther.2024.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Coukos R., Krainc D. Key genes and convergent pathogenic mechanisms in Parkinson disease. Nat. Rev. Neurosci. 2024;25:393–413. doi: 10.1038/s41583-024-00812-2. [DOI] [PubMed] [Google Scholar]
  7. Creekmore B. C., Watanabe R., Lee E. B. Neurodegenerative disease tauopathies. Ann. Rev. Pathol. 2024;19:345–370. doi: 10.1146/annurev-pathmechdis-051222-120750. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Dan K., Yoo J., Min H. The emerging threat of micro- and nanoplastics on the maturation and activity of immune cells. Biomol. Ther. (Seoul) 2025;33:95–105. doi: 10.4062/biomolther.2024.195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. de Oliveira R. B., Pelepenko L. E., Masaro D. A., Lustosa G. M., de Oliveira M. C., Roza N. A., Marciano M. A., Dos Reis L. M., Kamel S., Louvet L. Effects of microplastics on the kidneys: a narrative review. Kidney Int. 2024;106:400–407. doi: 10.1016/j.kint.2024.05.023. [DOI] [PubMed] [Google Scholar]
  10. Ehioghae M., Vippa T. K., Askins D., Slusarczyk S., Bobo E., Montoya A., Anderson D., Robinson C. L., Kaye A. D., Urits I. Exploring orthopedic stem-cell approaches for osteoarthritis management: current trends and future horizons. Curr. Pain Headache. Rep. 2024;28:27–35. doi: 10.1007/s11916-023-01191-6. [DOI] [PubMed] [Google Scholar]
  11. Goswami S., Adhikary S., Bhattacharya S., Agarwal R., Ganguly A., Nanda S., Rajak P. The alarming link between environmental microplastics and health hazards with special emphasis on cancer. Life Sci. 2024;355:122937. doi: 10.1016/j.lfs.2024.122937. [DOI] [PubMed] [Google Scholar]
  12. Han J. Y., Lee E.-H., Kim S.-M., Park C.-H. Efficient generation of dopaminergic neurons from mouse ventral midbrain astrocytes. Biomol. Ther. (Seoul) 2023a;31:264–275. doi: 10.4062/biomolther.2022.140. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Han S.-C., Kang J.-I., Choi Y. K., Boo H.-J., Yoon W.-J., Kang H.-K., Yoo E.-S. Intermittent fasting modulates immune response by generating tregs via TGF-β Dependent mechanisms in obese mice with allergic contact dermatitis. Biomol. Ther. (Seoul) 2023b;32:136–145. doi: 10.4062/biomolther.2023.053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hutchings C., Phillips J. A., Djamgoz M. B. Nerve input to tumours: pathophysiological consequences of a dynamic relationship. Biochim. Biophys. Acta Rev. Cancer. 2020;1874:188411. doi: 10.1016/j.bbcan.2020.188411. [DOI] [PubMed] [Google Scholar]
  15. Hwang J., Yoo J. A., Yoon H., Han T., Yoon J., An S., Cho J. Y., Lee J. The role of leptin in the association between obesity and psoriasis. Biomol. Ther. (Seoul) 2020;29:11–21. doi: 10.4062/biomolther.2020.054. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Jackson R. J., Hyman B. T., Serrano-Pozo A. Multifaceted roles of APOE in Alzheimer disease. Nat. Rev. Neurol. 2024;20:457–474. doi: 10.1038/s41582-024-00988-2. [DOI] [PubMed] [Google Scholar]
  17. Jeong Y.-H., Park J.-S., Kim D.-H., Kim H.-S. Lonchocarpine increases Nrf2/ARE-mediated antioxidant enzyme expression by modulating AMPK and MAPK signaling in brain astrocytes. Biomol. Ther. (Seoul) 2016;24:581–588. doi: 10.4062/biomolther.2016.141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Jung K. H., Kim S. E., Go H. G., Lee Y. J., Park M. S., Ko S., Han B. S., Yoon Y.-C., Cho Y. J., Lee P. Synergistic renoprotective effect of melatonin and zileuton by inhibition of ferroptosis via the AKT/mTOR/NRF2 signaling in kidney injury and fibrosis. Biomol. Ther. (Seoul) 2023;31:599–610. doi: 10.4062/biomolther.2023.062. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Kim E., Kim H. K., Sul J. H., Lee J., Baek S. H., Cho Y., Han J., Kim J., Park S., Park J. H. Extracellular vesicles derived from adipose stem cells alleviate systemic sclerosis by inhibiting tgf-β pathway. Biomol. Ther. (Seoul) 2024;32:432–441. doi: 10.4062/biomolther.2023.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Kim J. H., Choi Y., Lee S., Oh M. S. Probiotics as potential treatments for neurodegenerative diseases: a review of the evidence from in vivo to clinical trial. Biomol. Ther. (Seoul) 2025;33:54–74. doi: 10.4062/biomolther.2024.215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Kim M. K., Kim H. S. An overview of existing and emerging weight-loss drugs to target obesity-related complications: insights from clinical trials. Biomol. Ther. (Seoul) 2025;33:5–17. doi: 10.4062/biomolther.2024.228. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kim P. Understanding the Unfolded Protein Response (UPR) pathway: insights into neuropsychiatric disorders and therapeutic potentials. Biomol. Ther. (Seoul) 2024;32:183–191. doi: 10.4062/biomolther.2023.181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Korczyn A. D., Grinberg L. T. Is Alzheimer disease a disease? Nat. Rev. Neurol. 2024;20:245–251. doi: 10.1038/s41582-024-00940-4. [DOI] [PubMed] [Google Scholar]
  24. Kwon D., Zhang K., Paul K. C., Folle A. D., Del Rosario I., Jacobs J. P., Keener A. M., Bronstein J. M., Ritz B. Diet and the gut microbiome in patients with Parkinson's disease. NPJ Parkinsons Dis. 2024;10:89. doi: 10.1038/s41531-024-00681-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Lee B., Lee S. M., Song J. W., Choi J. W. Gut microbiota metabolite messengers in brain function and pathology at a view of cell type-based receptor and enzyme reaction. Biomol. Ther. (Seoul) 2024;32:403–423. doi: 10.4062/biomolther.2024.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Lee C. H., Cho J., Lee K. Tumour regression via integrative regulation of neurological, inflammatory, and hypoxic tumour microenvironment. Biomol. Ther. (Seoul) 2020;28:119–130. doi: 10.4062/biomolther.2019.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Lee H. J., Hossain R., Baek C., Lee C. J., Hwang S. Intra-articular injection of stem cells for the regeneration of knee joint cartilage: a therapeutic option for knee osteoarthritis - a narrative review. Biomol. Ther. (Seoul) 2025;33:86–94. doi: 10.4062/biomolther.2024.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Lefevre-Arbogast S., Chaker J., Mercier F., Barouki R., Coumoul X., Miller G., David A., Samieri C. Assessing the contribution of the chemical exposome to neurodegenerative disease. Nat. Neurosci. 2024;27:812–821. doi: 10.1038/s41593-024-01627-1. [DOI] [PubMed] [Google Scholar]
  29. Li C., Sun Y., Xu W., Chang F., Wang Y., Ding J. Mesenchymal stem cells-involved strategies for rheumatoid arthritis therapy. Adv. Sci. 2024;11:2305116. doi: 10.1002/advs.202305116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Liao X.-L., Chen Z.-F., Ou S.-P., Liu Q.-Y., Lin S.-H., Zhou J.-M., Wang Y., Cai Z. Neurological impairment is crucial for tire rubber-derived contaminant 6PPDQ-induced acute toxicity to rainbow trout. Sci. Bull. 2024;69:621–635. doi: 10.1016/j.scib.2023.12.045. [DOI] [PubMed] [Google Scholar]
  31. Liu Y., Cao Y., Li H., Liu H., Bi L., Chen Q., Peng R. A systematic review of microplastics emissions in kitchens: understanding the links with diseases in daily life. Environ. Int. 2024;188:108740. doi: 10.1016/j.envint.2024.108740. [DOI] [PubMed] [Google Scholar]
  32. Lyu Y., Xie F., Chen B., Shin W. S., Chen W., He Y., Leung K. T., Tse G. M., Yu J., To K. F. The nerve cells in gastrointestinal cancers: from molecular mechanisms to clinical intervention. Oncogene. 2024;43:77–91. doi: 10.1038/s41388-023-02909-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Mancusi R., Monje M. The neuroscience of cancer. Nature. 2023;618:467–479. doi: 10.1038/s41586-023-05968-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Morris H. R., Spillantini M. G., Sue C. M., Williams-Gray C. H. The pathogenesis of Parkinson's disease. Lancet. 2024;403:293–304. doi: 10.1016/S0140-6736(23)01478-2. [DOI] [PubMed] [Google Scholar]
  35. Müller T. D., Blüher M., Tschöp M. H., DiMarchi R. D. Anti-obesity drug discovery: advances and challenges. Nat. Rev. Drug Discov. 2022;21:201–223. doi: 10.1038/s41573-021-00337-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Natesan V., Kim S.-J. Diabetic nephropathy-a review of risk factors, progression, mechanism, and dietary management. Biomol. Ther. (Seoul) 2021;29:365–372. doi: 10.4062/biomolther.2020.204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Natesan V., Kim S. Natural compounds in kidney disease: therapeutic potential and drug development. Biomol. Ther. (Seoul) 2025;33:39–53. doi: 10.4062/biomolther.2024.142. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Ni Z., Zhou S., Li S., Kuang L., Chen H., Luo X., Ouyang J., He M., Du X., Chen L. Exosomes: roles and therapeutic potential in osteoarthritis. Bone Res. 2020;8:25. doi: 10.1038/s41413-020-0100-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Nixon R. A., Rubinsztein D. C. Mechanisms of autophagy-lysosome dysfunction in neurodegenerative diseases. Nat. Rev. Mol. Cell Biol. 2024;25:926–946. doi: 10.1038/s41580-024-00757-5. [DOI] [PubMed] [Google Scholar]
  40. Novikoff A., Grandl G., Liu X., Müller T. D. Why are we still in need for novel anti-obesity medications? Lancet Reg. Health Eur. 2024;47:101098. doi: 10.1016/j.lanepe.2024.101098. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Piao H., Yun J. M., Shin A., Cho B., Kang D. Comparing non-communicable disease risk factors in Asian migrants and native Koreans among the Asian population. Biomol. Ther. (Seoul) 2022;30:603–615. doi: 10.4062/biomolther.2022.036. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Penugurti V., Manne R. K., Bai L., Kant R., Lin H.-K. AMPK: the Energy Sensor at the Crossroads of Aging and Cancer. Elsevier; 2024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Poh A. The Nerve(s) of Cancer: A New Hallmark? 2024. doi: 10.1158/2159-8290.CD-NW2024-0028. [DOI] [Google Scholar]
  44. Pokhrel R. H., Acharya S., Mishra S., Gu Y., Manzoor U., Kim J.-K., Park Y., Chang J.-H. AMPK alchemy: therapeutic potentials in allergy, aging, and cancer. Biomol. Ther. (Seoul) 2024;32:171–182. doi: 10.4062/biomolther.2023.222. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Raza S., Rajak S., Yen P. M., Sinha R. A. Autophagy and hepatic lipid metabolism: mechanistic insight and therapeutic potential for MASLD. NPJ Metab. Health Dis. 2024;2:19. doi: 10.1038/s44324-024-00022-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Rho S. B., Byun H. J., Kim B.-R., Lee C. H. Knockdown of LKB1 sensitizes endometrial cancer cells via AMPK activation. Biomol. Ther. (Seoul) 2021;29:650–657. doi: 10.4062/biomolther.2021.131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Seo D.-O., Holtzman D. M. Current understanding of the Alzheimer's disease-associated microbiome and therapeutic strategies. Exp. Mol. Med. 2024;56:86–94. doi: 10.1038/s12276-023-01146-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Sun H., Yang B., Li Q., Zhu X., Song E., Liu C., Song Y., Jiang G. Polystyrene nanoparticles trigger aberrant condensation of TDP-43 and amyotrophic lateral sclerosis-like symptoms. Nat. Nanotechnol. 2024;19:1354–1365. doi: 10.1038/s41565-024-01683-5. [DOI] [PubMed] [Google Scholar]
  49. Sun J., Pan J., Liu Q., Cheng J., Tang Q., Ji Y., Cheng K., Liu L., Wang D., Wu N. Melatonin attenuates mitochondrial damage in aristolochic acid-induced acute kidney injury. Biomol. Ther. (Seoul) 2022;31:97–107. doi: 10.4062/biomolther.2022.054. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Tian R., Su S., Yu Y., Liang S., Ma C., Jiao Y., Xing W., Tian Z., Jiang T., Wang J. Revolutionizing osteoarthritis treatment: How mesenchymal stem cells hold the key. Biomed. Pharmacother. 2024;173:116458. doi: 10.1016/j.biopha.2024.116458. [DOI] [PubMed] [Google Scholar]
  51. Wada J., Makino H. Innate immunity in diabetes and diabetic nephropathy. Nat. Rev. Nephrol. 2016;12:13–26. doi: 10.1038/nrneph.2015.175. [DOI] [PubMed] [Google Scholar]
  52. Winkler F., Venkatesh H. S., Amit M., Batchelor T., Demir I. E., Deneen B., Gutmann D. H., Hervey-Jumper S., Kuner T., Mabbott D. Cancer neuroscience: state of the field, emerging directions. Cell. 2023;186:1689–1707. doi: 10.1016/j.cell.2023.02.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Xu W., Liu J., Zhang J., Lu J., Guo J. Tumor microenvironment crosstalk between tumors and the nervous system in pancreatic cancer: molecular mechanisms and clinical perspectives. Biochim. Biophys. Acta Rev. Cancer. 2024;1879:189032. doi: 10.1016/j.bbcan.2023.189032. [DOI] [PubMed] [Google Scholar]
  54. Yajing M., Sufang L., Qingfeng Z., Zhonghua L., Zhang Z., Bin Y. Approved drugs and natural products at clinical stages for treating Alzheimer's disease. Chin. J. Nat. Med. 2024;22:699–710. doi: 10.1016/S1875-5364(24)60606-0. [DOI] [PubMed] [Google Scholar]
  55. Zhao J., Adiele N., Gomes D., Malovichko M., Conklin D. J., Ekuban A., Luo J., Gripshover T., Watson W. H., Banerjee M. Obesogenic polystyrene microplastic exposures disrupt the gut-liver-adipose axis. Toxicol. Sci. 2024;198:210–220. doi: 10.1093/toxsci/kfae013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Zheng P. C., Li R., Lai K. P., Zhang X. X. Biological exposure to microplastics and nanoplastics and plastic additives: impairment of glycolipid metabolism and adverse effects on metabolic diseases. Environ. Sci. Pollut. Res. 2024;31:60778–60791. doi: 10.1007/s11356-024-35220-7. [DOI] [PubMed] [Google Scholar]

Articles from Biomolecules & Therapeutics are provided here courtesy of Korean Society of Applied Pharmacology

RESOURCES