A mini review of noncoding RNAs in the pathogenesis of polycystic kidney disease

Mengsi Hu , Zongze Li

Journal of Translational Genetics and Genomics ›› 2025, Vol. 9 ›› Issue (2) : 100 -113.

PDF
Journal of Translational Genetics and Genomics ›› 2025, Vol. 9 ›› Issue (2) :100 -113. DOI: 10.20517/jtgg.2025.12
review-article

A mini review of noncoding RNAs in the pathogenesis of polycystic kidney disease

Author information +
History +
PDF

Abstract

Polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys, leading to kidney enlargement and progressive renal failure. Recent advances have indicated a pivotal role of noncoding RNAs (ncRNAs), including microRNAs (miRNAs), long noncoding RNAs (lncRNAs), circular RNAs (circRNAs) and PIWI-interacting RNAs (piRNAs), in the pathogenesis of PKD, potentially through regulating gene expression and cellular processes related to cyst formation, inflammation, and fibrosis. This review summarizes current knowledge of noncoding RNAs, explores their potential as biomarkers and therapeutic targets, and proposes potential directions for future research to further elucidate their roles in disease progression.

Keywords

Noncoding RNA / polycystic kidney disease / therapeutic target / miRNA / lncRNA / gene expression / signaling pathway

Cite this article

Download citation ▾
Mengsi Hu, Zongze Li. A mini review of noncoding RNAs in the pathogenesis of polycystic kidney disease. Journal of Translational Genetics and Genomics, 2025, 9(2): 100-113 DOI:10.20517/jtgg.2025.12

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

ChakrabortyA.Prospects for gene therapy in polycystic kidney disease.Curr Opin Nephrol Hypertens2025;34:121-7 PMCID:PMC11606769

[2]

BergmannC,HarrisPC,PetersDJM.Polycystic kidney disease.Nat Rev Dis Primers2018;4:50 PMCID:PMC6592047

[3]

MuñozJJ,AmaralAG.Identification of housekeeping genes for microRNA expression analysis in kidney tissues of Pkd1 deficient mouse models.Sci Rep2020;10:231 PMCID:PMC6959247

[4]

Gall E, Torres VE, Harris PC. Genetic complexity of autosomal dominant polycystic kidney and liver diseases.J Am Soc Nephrol2018;29:13-23 PMCID:PMC5748917

[5]

TsaiYC,JiangST,ChiouYY.Safe nanocomposite-mediated efficient delivery of MicroRNA plasmids for autosomal dominant polycystic kidney disease (ADPKD) therapy.Adv Healthc Mater2019;8:e1801358

[6]

Gall E, Alam A, Perrone RD. Autosomal dominant polycystic kidney disease.Lancet2019;393:919-35

[7]

JdiaaSS,YuASL.Treatment of autosomal-dominant polycystic kidney disease.Am J Kidney Dis2025;85:491-500

[8]

YheskelM.Therapeutic microRNAs in polycystic kidney disease.Curr Opin Nephrol Hypertens2017;26:282-9 PMCID:PMC6343829

[9]

WooYM.microRNA biomarkers in cystic diseases.BMB Rep2013;46:338-45 PMCID:PMC4133917

[10]

IglesiasCG,OffordKP,BeardCM.Epidemiology of adult polycystic kidney disease, Olmsted County, Minnesota: 1935-1980.Am J Kidney Dis1983;2:630-9

[11]

DalgaardOZ.Bilateral polycystic disease of the kidneys; a follow-up of two hundred and eighty-four patients and their families.Acta Med Scand Suppl1957;328:1-255

[12]

WangS,XieH.PKD2: An important membrane protein in organ development.Cells2024;13:1722 PMCID:PMC11506562

[13]

González-PerrettS,IbarraC.Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel.Proc Natl Acad Sci U S A2001;98:1182-7

[14]

KoulenP,GengL.Polycystin-2 is an intracellular calcium release channel.Nat Cell Biol2002;4:191-7

[15]

KleeneSJ.The native TRPP2-dependent channel of murine renal primary cilia.Am J Physiol Renal Physiol2017;312:F96-108 PMCID:PMC5283891

[16]

LiuX,DuanJ,DeCaenPG.Polycystin-2 is an essential ion channel subunit in the primary cilium of the renal collecting duct epithelium.Elife2018;7:e33183 PMCID:PMC5812715

[17]

KöttgenM,Garcia-GonzalezMA.TRPP2 and TRPV4 form a polymodal sensory channel complex.J Cell Biol2008;182:437-47 PMCID:PMC2500130

[18]

DjenouneL,TruongTV.Cilia function as calcium-mediated mechanosensors that instruct left-right asymmetry.Science2023;379:71-8 PMCID:PMC9939240

[19]

KatohTA,MizunoK.Immotile cilia mechanically sense the direction of fluid flow for left-right determination.Science2023;379:66-71

[20]

ChowdhuryP,PoddarA,ChenQ.The Mechanosensitive Pkd2 channel modulates the recruitment of myosin II and actin to the cytokinetic contractile ring.J Fungi2024;10:455 PMCID:PMC11277609

[21]

ZhouJX.Non-coding RNAs in hereditary kidney disorders.Int J Mol Sci2021;22:3014 PMCID:PMC7998154

[22]

TorresVE.Pro: Tolvaptan delays the progression of autosomal dominant polycystic kidney disease.Nephrol Dial Transplant2019;34:30-4 PMCID:PMC6657439

[23]

LuH,OttE.Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease.Nat Genet2017;49:1025-34

[24]

GoggolidouP.The genetics of autosomal recessive polycystic kidney disease (ARPKD).Biochim Biophys Acta Mol Basis Dis2022;1868:166348

[25]

MallawaarachchiAC,HortY.Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing.Eur J Hum Genet2021;29:760-70

[26]

WilsonEM,TorresVE,BesseW.Large Deletions in GANAB and SEC63 explain 2 cases of polycystic kidney and liver disease.Kidney Int Rep2020;5:727-31 PMCID:PMC7210741

[27]

Sutters M. Polycystic Kidney Disease, Autosomal Dominant. In: Ganten D, Ruckpaul K, Birchmeier W, et al., editors. Encyclopedic reference of genomics and proteomics in molecular medicine. Berlin, Heidelberg: Springer; 2005. pp. 1435-9. Available from: https://link.springer.com/referenceworkentry/10.1007/3-540-29623-9_1380#citeas [accessed 29 May 2025].

[28]

PorathB,Cornec-LeGall E.Genkyst Study GroupHALT Progression of Polycystic Kidney Disease GroupConsortium for Radiologic Imaging Studies of Polycystic Kidney DiseaseMutations in GANAB, encoding the glucosidase IIα subunit, cause autosomal-dominant polycystic kidney and liver disease.Am J Hum Genet2016;98:1193-207

[29]

BolettaA.Physiologic mechanisms underlying polycystic kidney disease.Physiol Rev2025;105:1553-607

[30]

SenumSR,BensonKA.Genomics England Research Consortiumthe HALT PKDCRISPDIPAKADPKD Modifierand TAME PKD studiesMonoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype.Am J Hum Genet2022;109:136-56 PMCID:PMC8764120

[31]

DordoniC,TosoD.Monoallelic pathogenic IFT140 variants are a common cause of autosomal dominant polycystic kidney disease-spectrum phenotype.Clin Kidney J2024;17:sfae026

[32]

SergiCM,HagerJ.Autosomal dominant polycystic kidney disease-related multifocal renal cell carcinoma: a narrative iconographic review.Int J Mol Sci2025;26:3965 PMCID:PMC12072103

[33]

ArmourEA,EssKC.Cystogenesis and elongated primary cilia in Tsc1-deficient distal convoluted tubules.Am J Physiol Renal Physiol2012;303:F584-92 PMCID:PMC3423116

[34]

HalbritterJ,DiazKA.GPN Study GroupIdentification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy.Hum Genet2013;132:865-84 PMCID:PMC4643834

[35]

LiX.Epigenetics and cell cycle regulation in cystogenesis.Cell Signal2020;68:109509 PMCID:PMC8154103

[36]

ShaoA,IgarashiP.Role of transcription factor hepatocyte nuclear factor-1β in polycystic kidney disease.Cell Signal2020;71:109568 PMCID:PMC7183897

[37]

Ruiz-ManriquezLM,Medina-GomezD.A brief review on the regulatory roles of microRNAs in Cystic diseases and their use as potential biomarkers.Genes2022;13:191 PMCID:PMC8872411

[38]

PhuaYL.MicroRNAs in the pathogenesis of cystic kidney disease.Curr Opin Pediatr2015;27:219-26 PMCID:PMC4409326

[39]

PandeyP,HoJ,KreidbergJA.Systems biology approach to identify transcriptome reprogramming and candidate microRNA targets during the progression of polycystic kidney disease.BMC Syst Biol2011;5:56 PMCID:PMC3111376

[40]

MacDonaldBT,HeX.Wnt/beta-catenin signaling: components, mechanisms, and diseases.Dev Cell2009;17:9-26 PMCID:PMC2861485

[41]

LinF,CordesK.Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease.Proc Natl Acad Sci U S A2003;100:5286-91 PMCID:PMC154337

[42]

KimS,NesinV.The polycystin complex mediates Wnt/Ca2+ signalling.Nat Cell Biol2016;18:752-64 PMCID:PMC4925210

[43]

LalM,PluznickJL.Polycystin-1 C-terminal tail associates with beta-catenin and inhibits canonical Wnt signaling.Hum Mol Genet2008;17:3105-17

[44]

deStephanis L,ServelloM.MicroRNA501-5p induces p53 proteasome degradation through the activation of the mTOR/MDM2 pathway in ADPKD cells.J Cell Physiol2018;233:6911-24

[45]

MargariaJP,DeSantis MC,FrancoI.The PI3K/Akt/mTOR pathway in polycystic kidney disease: A complex interaction with polycystins and primary cilium.Cell Signal2020;66:109468

[46]

DereR,SandfordRN.Carboxy terminal tail of polycystin-1 regulates localization of TSC2 to repress mTOR.PLoS One2010;5:e9239 PMCID:PMC2821926

[47]

AlzahraniOR,AlharbiAA.Identification and characterization of novel mutations in chronic kidney disease (CKD) and autosomal dominant polycystic kidney disease (ADPKD) in saudi subjects by whole-exome sequencing.Medicina2022;58:1657 PMCID:PMC9692281

[48]

MostovKE.mTOR is out of control in polycystic kidney disease.Proc Natl Acad Sci U S A2006;103:5247-8 PMCID:PMC1459339

[49]

LiuY,WangX.Dual mTOR/PI3K inhibition limits PI3K-dependent pathways activated upon mTOR inhibition in autosomal dominant polycystic kidney disease.Sci Rep2018;8:5584 PMCID:PMC5882886

[50]

ZhangL,ZhouJX,CalvetJP.RNA helicase p68 inhibits the transcription and post-transcription of Pkd1 in ADPKD.Theranostics2020;10:8281-97

[51]

AliH,Abu-FarhaM.Global analysis of urinary extracellular vesicle small RNAs in autosomal dominant polycystic kidney disease.J Gene Med2024;26:e3674

[52]

MariottiV,CadamuroM,StrazzaboscoM.New insights on the role of vascular endothelial growth factor in biliary pathophysiology.JHEP Rep2021;3:100251 PMCID:PMC8189933

[53]

LeiererJ,HoferB.Coregulation analysis of mechanistic biomarkers in autosomal dominant polycystic kidney disease.Int J Mol Sci2021;22:6885 PMCID:PMC8269435

[54]

CobanM.The association of serum angiogenic growth factors with renal structure and function in patients with adult autosomal dominant polycystic kidney disease.Int Urol Nephrol2018;50:1293-300

[55]

LeeEJ,KimJW.TAZ/Wnt-β-catenin/c-MYC axis regulates cystogenesis in polycystic kidney disease.Proc Natl Acad Sci U S A2020;117:29001-12 PMCID:PMC7682393

[56]

LakhiaR,BiggersL.Enhancer and super-enhancer landscape in polycystic kidney disease.Kidney Int2023;103:87-99 PMCID:PMC9841439

[57]

FoxJC,HassanF,HaffnerD.Defects of renal tubular homeostasis and cystogenesis in the Pkhd1 knockout.iScience2024;27:109487 PMCID:PMC10973142

[58]

RamalingamH,PatelV.Modulation of polycystic kidney disease by non-coding RNAs.Cell Signal2020;71:109548 PMCID:PMC7183876

[59]

FragiadakiM.Lessons from microRNA biology: top key cellular drivers of autosomal dominant polycystic kidney disease.Biochim Biophys Acta Mol Basis Dis2022;1868:166358

[60]

CarneyEF.Polycystic kidney disease: microRNA-17: a new drug target for ADPKD.Nat Rev Nephrol2017;13:260

[61]

HajarnisS,YheskelM.microRNA-17 family promotes polycystic kidney disease progression through modulation of mitochondrial metabolism.Nat Commun2017;8:14395 PMCID:PMC5316862

[62]

LeeSO,SplinterP.MicroRNA15a modulates expression of the cell-cycle regulator Cdc25A and affects hepatic cystogenesis in a rat model of polycystic kidney disease.J Clin Invest2008;118:3714-24 PMCID:PMC2571032

[63]

YheskelM,Cobo-StarkP,PatelV.Anti-microRNA screen uncovers miR-17 family within miR-17~92 cluster as the primary driver of kidney cyst growth.Sci Rep2019;9:1920 PMCID:PMC6374450

[64]

WooYM,KooNJ.Profiling of miRNAs and target genes related to cystogenesis in ADPKD mouse models.Sci Rep2017;7:14151 PMCID:PMC5658336

[65]

LakhiaR,WilliamsD.MicroRNA-21 aggravates cyst growth in a model of polycystic kidney disease.J Am Soc Nephrol2016;27:2319-30 PMCID:PMC4978047

[66]

DweepH,KharkarA,GretzN.Parallel analysis of mRNA and microRNA microarray profiles to explore functional regulatory patterns in polycystic kidney disease: using PKD/Mhm rat model.PLoS One2013;8:e53780 PMCID:PMC3542345

[67]

SunL,WuM.Inhibition of MiR-199a-5p reduced cell proliferation in autosomal dominant polycystic kidney disease through targeting CDKN1C.Med Sci Monit2015;21:195-200 PMCID:PMC4304454

[68]

LaiS,PerrottaAM.MicroRNA and renal fibrosis in autosomal dominant polycystic kidney disease: a longitudinal study.J Nephrol2025;38:153-62 PMCID:PMC11903767

[69]

SunL,WangZ.MiR-182 inhibits kidney fibrosis by regulating transforming growth factor β1/Smad3 pathway in autosomal dominant polycystic kidney disease.IUBMB Life2020;72:1340-8

[70]

ChuAS.A role for microRNA in cystic liver and kidney diseases.J Clin Invest2008;118:3585-7 PMCID:PMC2571036

[71]

KimDY,LeeS.Impact of miR-192 and miR-194 on cyst enlargement through EMT in autosomal dominant polycystic kidney disease.FASEB J2019;33:2870-84

[72]

WesselyO.Small RNAs have a big effect on polycystic kidney disease.J Am Soc Nephrol2012;23:1909-10 PMCID:PMC3507373

[73]

HajarnisSS,AboudehenK.Transcription factor hepatocyte nuclear factor-1β (HNF-1β) regulates microRNA-200 expression through a long noncoding RNA.J Biol Chem2015;290:24793-805 PMCID:PMC4598991

[74]

BoutetA,MaxwellPH,RomeroJ.Snail activation disrupts tissue homeostasis and induces fibrosis in the adult kidney.EMBO J2006;25:5603-13 PMCID:PMC1679761

[75]

AboudehenK,Cobo-StarkP.Hepatocyte nuclear factor-1β regulates urinary concentration and response to hypertonicity.J Am Soc Nephrol2017;28:2887-900

[76]

ShinY,KoJY,ParkJH.Regulation of KLF12 by microRNA-20b and microRNA-106a in cystogenesis.FASEB J2018;32:3574-82

[77]

EckbergK,ButtramD,IgarashiP.Small hairpin inhibitory RNA delivery in the metanephric organ culture identifies long noncoding RNA Pvt1 as a modulator of cyst growth.Am J Physiol Renal Physiol2022;323:F335-48 PMCID:PMC9423782

[78]

AboudehenK,KanchwalaM.Long noncoding RNA Hoxb3os is dysregulated in autosomal dominant polycystic kidney disease and regulates mTOR signaling.J Biol Chem2018;293:9388-98 PMCID:PMC6005429

[79]

YangY,WeiF.Silencing of long non-coding RNA H19 downregulates CTCF to protect against atherosclerosis by upregulating PKD1 expression in ApoE knockout mice.Aging (Albany NY)2019;11:10016-30 PMCID:PMC6914395

[80]

WeisserI,D’AmicoS,AboudehenK.Ablation of long noncoding RNA Hoxb3os exacerbates cystogenesis in mouse polycystic kidney disease.J Am Soc Nephrol2024;35:41-55 PMCID:PMC10786614

[81]

WangX.Down-regulation of lncRNA-NEAT1 alleviated the non-alcoholic fatty liver disease via mTOR/S6K1 signaling pathway.J Cell Biochem2018;119:1567-74

[82]

SongP,LiuZ.LncRNA MALAT1 aggravates renal tubular injury via activating LIN28A and the Nox4/AMPK/mTOR signaling axis in diabetic nephropathy.Front Endocrinol2022;13:895360 PMCID:PMC9259889

[83]

LakhiaR,FlatenA.Interstitial microRNA miR-214 attenuates inflammation and polycystic kidney disease progression.JCI Insight2020;5:e133785 PMCID:PMC7205276

[84]

ChenLL.The biogenesis and emerging roles of circular RNAs.Nat Rev Mol Cell Biol2016;17:205-11

[85]

Zonneveld AJ, Kölling M, Bijkerk R, Lorenzen JM. Circular RNAs in kidney disease and cancer.Nat Rev Nephrol2021;17:814-26

[86]

LiY.Circ_0040994 depletion alleviates lipopolysaccharide-induced HK2 cell injury through miR-17-5p/TRPM7 axis.Environ Toxicol2023;38:2585-94

[87]

KongH,QiD.circ_0002970 promotes fibroblast-like synoviocytes invasion and the inflammatory response through Hippo/YAP signaling to induce CTGF/CCN1 expression in rheumatoid arthritis.Arthritis Res Ther2025;27:97 PMCID:PMC12023364

[88]

GuptaG,GoyalA.piRNAs in leukemogenesis: Mechanisms, biomarkers, and therapeutic implications.Clin Chim Acta2025;571:120220

[89]

AliH,Abu-FarhaM.Dysregulated urinary extracellular vesicle small RNAs in diabetic nephropathy: implications for diagnosis and therapy.J Endocr Soc2024;8:bvae114 PMCID:PMC11222982

[90]

’tHart LM,BoulandGA.Small RNA sequencing reveals snoRNAs and piRNA-019825 as novel players in diabetic kidney disease.Endocrine2024;86:194-203 PMCID:PMC11445283

[91]

XuY,ZhangY.piRNAs and circRNAs acting as diagnostic biomarkers in clear cell renal cell carcinoma.Sci Rep2025;15:7774 PMCID:PMC11882777

[92]

KocyigitI,SenerEF.Serum micro-rna profiles in patients with autosomal dominant polycystic kidney disease according to hypertension and renal function.BMC Nephrol2017;18:179 PMCID:PMC5450105

[93]

KocyigitI,UysalC.Predicting progression of autosomal dominant polycystic kidney disease by changes in the telomeric epigenome.Cells2022;11:3300 PMCID:PMC9600909

[94]

MagayrTA,StreetsAJ.Global microRNA profiling in human urinary exosomes reveals novel disease biomarkers and cellular pathways for autosomal dominant polycystic kidney disease.Kidney Int2020;98:420-35

[95]

GhanemA,MunairdjyDebeh FG.Biomarkers of kidney disease progression in ADPKD.Kidney Int Rep2024;9:2860-82 PMCID:PMC11492289

[96]

HavensMA,RigoF.Elevating microRNA levels by targeting biogenesis with steric-blocking antisense oligonucleotides.RNA2024;30:1543-53 PMCID:PMC11571803

[97]

KuleszaA,FliszkiewiczM,PączekL.miRNA-16 as a predictive factor for intracranial aneurysms in autosomal dominant polycystic kidney disease.Neurol Neurochir Pol2021;55:306-9

[98]

SzetoCC,PoonPY.Urinary long non-coding RNA levels as biomarkers of lupus nephritis.Int J Mol Sci2023;24:11813 PMCID:PMC10380660

[99]

DieterC,GirardiE.The lncRNA MALAT1 is upregulated in urine of type 1 diabetes mellitus patients with diabetic kidney disease.Genet Mol Biol2023;46:e20220291 PMCID:PMC10240573

[100]

XieZ,ZhouG.Urinary circular RNA panels to detect HBV-related hepatocellular carcinoma: a multicenter, large-scale, case-control study.J Natl Compr Canc Netw2024;23:e247058

[101]

PatelV,HajarnisS.miR-17~92 miRNA cluster promotes kidney cyst growth in polycystic kidney disease.Proc Natl Acad Sci U S A2013;110:10765-70

[102]

LeeEC,AllersonC.Discovery and preclinical evaluation of anti-miR-17 oligonucleotide RGLS4326 for the treatment of polycystic kidney disease.Nat Commun2019;10:4148 PMCID:PMC6742637

[103]

Regulus therapeutics announces positive clinical and regulatory updates from its autosomal dominant polycystic kidney disease (ADPKD) program for farabursen (RGLS8429). 2025. Available from: https://www.prnewswire.com/news-releases/regulus-therapeutics-announces-positive-clinical-and-regulatory-updates-from-its-autosomal-dominant-polycystic-kidney-disease-adpkd-program-for-farabursen-rgls8429-302362731.html [accessed 28 May 2025]

[104]

PapiC,ZurloM,GambariR.The cystic fibrosis transmembrane conductance regulator gene (CFTR) is under post-transcriptional control of microRNAs: analysis of the effects of agomiRNAs mimicking miR-145-5p, miR-101-3p, and miR-335-5p.Noncoding RNA2023;9:29 PMCID:PMC10146138

[105]

PersuA,LannoyN.CF gene and cystic fibrosis transmembrane conductance regulator expression in autosomal dominant polycystic kidney disease.J Am Soc Nephrol2000;11:2285-96

[106]

YandaMK,CebotaruL.Therapeutic potential for CFTR correctors in autosomal recessive polycystic kidney disease.Cell Mol Gastroenterol Hepatol2021;12:1517-29 PMCID:PMC8529398

[107]

NiemczykM,GromadkaA,PączekL.Potential role of plant microRNAs in the pathogenesis of autosomal dominant polycystic kidney disease: an in silico study.Pol Arch Intern Med2021;131:306-8

[108]

HinoT,NakagawaR.An AsCas12f-based compact genome-editing tool derived by deep mutational scanning and structural analysis.Cell2023;186:4920-4935.e23

[109]

ChenH,GuoJ.Branched chemically modified poly(A) tails enhance the translation capacity of mRNA.Nat Biotechnol2025;43:194-203 PMCID:PMC11416571

[110]

JerusalinskyD,EpsteinAL.Herpes simplex virus type 1-based amplicon vectors for fundamental research in neurosciences and gene therapy of neurological diseases.J Physiol Paris2012;106:2-11

[111]

AulicinoF,ToelzerC.Highly efficient CRISPR-mediated large DNA docking and multiplexed prime editing using a single baculovirus.Nucleic Acids Res2022;50:7783-99 PMCID:PMC9303279

[112]

ZhuJ,MahalingamM.A prokaryotic-eukaryotic hybrid viral vector for delivery of large cargos of genes and proteins into human cells.Sci Adv2019;5:eaax0064 PMCID:PMC6703872

[113]

ZhengQ,EcclesMR.Non-coding RNAs as potential biomarkers and therapeutic targets in polycystic kidney disease.Front Physiol2022;13:1006427 PMCID:PMC9531119

[114]

SubhashS,ParmarA,SimmonsJ.Reactive oxygen species in cystic kidney disease.Antioxidants2024;13:1186 PMCID:PMC11504974

AI Summary AI Mindmap
PDF

47

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/