# Exploring the Dermatological Benefits of Coffee Extracts and Their Derivatives

**Authors:** Hsiao-Fang Liao, Po-Yuan Wu, Kuo-Ching Wen, Tsen-Jung Lin, Hung-Lung Chiang, Hsiu-Mei Chiang

PMC · DOI: 10.3390/antiox15020244 · Antioxidants · 2026-02-12

## TL;DR

Coffee extracts show potential for skin health due to their antioxidant and anti-inflammatory properties, but more clinical research is needed to confirm their effectiveness.

## Contribution

This review systematically evaluates the dermatological potential of coffee-derived materials and highlights translational barriers.

## Key findings

- In vitro and animal studies show antioxidant, anti-aging, and wound-healing effects of coffee extracts.
- Human trials report modest improvements in skin hydration and barrier function, but with methodological limitations.
- Observational studies suggest a possible link between coffee consumption and reduced skin cancer risk, though causality is unproven.

## Abstract

Coffee-derived materials from diverse botanical sources (beans, leaves, fruit and spent grounds) contain bioactive polyphenolic compounds, alkaloids, and diterpenes with potential dermatological applications. This review critically evaluates evidence quality across study designs. In vitro studies demonstrate antioxidant, anti-aging, anti-inflammatory, photoprotective, wound-healing, and antimicrobial activities. Animal models show photoprotection and wound-healing effects. These studies highlight the multifunctional dermatological value of coffee-derived materials as ingredients for cosmetic and therapeutic formulations aimed at combating skin aging, inflammation, and barrier dysfunction. Limited human trials (typically small sample sizes and short duration) report modest improvements in skin hydration, elasticity, barrier function, and reductions in erythema, transepidermal water loss, and ultraviolet-induced damage, though methodological limitations constrain interpretation. Observational epidemiological studies report inverse associations between coffee consumption and melanoma/basal cell carcinoma risk, but residual confounding by sun exposure, lifestyle factors, and genetic susceptibility precludes causal inference. Critical translational barriers include insufficient pharmacokinetic characterization, inadequate extract standardization across sources and processing methods, formulation challenges, bioavailability uncertainties, and limited independent validation. While preclinical evidence supports diverse biological activities and suggests multifunctional potential for cosmetic and therapeutic applications, current evidence remains insufficient to recommend coffee-derived products as a primary evidence-based dermatological intervention. Overall, large-scale, independent clinical trials with adequate duration and clinically meaningful endpoints are essential for translating laboratory findings into validated clinical applications.

## Linked entities

- **Diseases:** melanoma (MONDO:0005105), basal cell carcinoma (MONDO:0005341)

## Full-text entities

- **Genes:** Oga (O-GlcNAcase) [NCBI Gene 76055] {aka Hy5, Mgea5, Ncoat}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Nbas (neuroblastoma amplified sequence) [NCBI Gene 71169] {aka 4933425L03Rik, Nag}, Mmp9 (matrix metallopeptidase 9) [NCBI Gene 17395] {aka B/MMP9, Clg4b, Gel B, MMP-9, pro-MMP-9}, GSTT1 (glutathione S-transferase theta 1) [NCBI Gene 2952], Cd207 (CD207 antigen) [NCBI Gene 246278], Fn1 (fibronectin 1) [NCBI Gene 14268] {aka E330027I09, Fn, Fn-1}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 17709], S100a1 (S100 calcium binding protein A1) [NCBI Gene 20193] {aka S100, S100a}, Mmp2 (matrix metallopeptidase 2) [NCBI Gene 17390] {aka Clg4a, GelA, MMP-2}, Acta2 (actin alpha 2, smooth muscle, aorta) [NCBI Gene 11475] {aka 0610041G09Rik, Actvs, SMAalpha, SMalphaA, a-SMA, alphaSMA}, JUND (JunD proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3727] {aka AP-1}, Dct (dopachrome tautomerase) [NCBI Gene 13190] {aka DT, TRP-2, TRP2, Tyrp-2, Tyrp2, slaty}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Cat (catalase) [NCBI Gene 12359] {aka 2210418N07, Cas-1, Cas1, Cs-1}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Flg (filaggrin) [NCBI Gene 14246] {aka ft}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, TNFRSF1A (TNF receptor superfamily member 1A) [NCBI Gene 7132] {aka CD120a, FPF, TBP1, TNF-R, TNF-R-I, TNF-R55}, MAPK14 (mitogen-activated protein kinase 14) [NCBI Gene 1432] {aka CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2}, Cxcl15 (C-X-C motif chemokine ligand 15) [NCBI Gene 20309] {aka Il8, Scyb15, lungkine, weche}, Ptgs2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 19225] {aka COX2, Cox-2, PES-2, PGHS-2, PHS II, PHS-2}, GSTK1 (glutathione S-transferase kappa 1) [NCBI Gene 373156] {aka GST, GST 13-13, GST13, GST13-13, GSTK1-1, hGSTK1}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, GSTM1 (glutathione S-transferase mu 1) [NCBI Gene 2944] {aka GST1, GSTM1-1, GSTM1a-1a, GSTM1b-1b, GTH4, GTM1}, Casp1 (caspase 1) [NCBI Gene 12362] {aka ICE, Il1bc}, Mmp13 (matrix metallopeptidase 13) [NCBI Gene 17386] {aka Clg, MMP-13, Mmp1}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, Tslp (thymic stromal lymphopoietin) [NCBI Gene 53603], Tyr (tyrosinase) [NCBI Gene 22173] {aka Oca1, albino, c, skc35}, Nos2 (nitric oxide synthase 2, inducible) [NCBI Gene 18126] {aka MAC-NOS, NOS-II, Nos-2, Nos2a, i-NOS, iNOS}, IFNR (interferon production regulator) [NCBI Gene 3466] {aka IFNGM, IFNGM2}, Nlrp3 (NLR family, pyrin domain containing 3) [NCBI Gene 216799] {aka AGTAVPRL, AII/AVP, Cias1, FCAS, FCU, MWS}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, CAT (catalase) [NCBI Gene 847], TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, Mpo (myeloperoxidase) [NCBI Gene 17523] {aka mKIAA4033}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599] {aka JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8}, Trp2 (tRNA proline 2) [NCBI Gene 104042] {aka Trp-2}, Cldn1 (claudin 1) [NCBI Gene 12737], Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, col-64 (Nematode cuticle collagen N-terminal domain-containing protein) [NCBI Gene 186127]
- **Diseases:** psoriasis (MESH:D011565), xerotic (MESH:C536156), carcinogenesis (MESH:D063646), hair loss (MESH:D000505), Skin Cancer (MESH:D012878), edema (MESH:D004487), irritation (MESH:D001523), water loss (MESH:D000069578), ear edema (MESH:D004427), Cancer (MESH:D009369), inflammatory dermatoses (MESH:D012871), injury to (MESH:D014947), Cutaneous inflammation (MESH:D007249), melanoma (MESH:D008545), inflammatory skin disorders (MESH:D012868), erythema (MESH:D004890), epidermal hyperplasia (MESH:D006965), BCC (MESH:D002280), atopic dermatitis (MESH:D003876), Cutaneous melanoma (MESH:C562393), sunburn (MESH:D013471), nevi (MESH:D009506), carcinogenic (MESH:D011230)
- **Chemicals:** ethanol (MESH:D000431), NO (MESH:D009569), Feruloylquinic acids (MESH:C420868), xanthone (MESH:C009689), Mangiferin (MESH:C013592), Alkaloids (MESH:D000470), vitamin C (MESH:D001205), SDS (MESH:D012967), CPDs (MESH:D011740), kahweol (MESH:C053401), phenolic acids (MESH:C017616), Isomangiferin (MESH:C061492), essential oils (MESH:D009822), catechin (MESH:D002392), Terpenoids (MESH:D013729), Xanthones (MESH:D044004), phenol (MESH:D019800), water (MESH:D014867), 2,2'-diphenyl-1-picrylhydrazyl (MESH:C004931), beta-(1,3)-glucan (MESH:C033363), chitin (MESH:D002686), HOCl (MESH:D006997), dicaffeoylquinic acids (MESH:C472707), rutin (MESH:D012431), quercetin (MESH:D011794), melanoidins (MESH:C011908), chitosan (MESH:D048271), carrageenan (MESH:D002351), croton oil (MESH:D003436), Trigonelline (MESH:C009560), histamine (MESH:D006632), 3-caffeoylquinic acid (MESH:D002726), Flavonoids (MESH:D005419), diterpenes (MESH:D004224), heavy metal (MESH:D019216), 2,4-dinitrochlorobenzene (MESH:D004137), ROS (MESH:D017382), anthocyanins (MESH:D000872), LPS (MESH:D008070), lipid (MESH:D008055), 2,2'-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid (MESH:C002502), melanin (MESH:D008543), sesquiterpenes (MESH:D012717), polyphenol (MESH:D059808), monoterpenes (MESH:D039821), oil (MESH:D009821), ergosterol (MESH:D004875), Procyanidins (MESH:D044945), Caffeine (MESH:D002110), 5-caffeoylquinic acid (-), O2 - (MESH:D013481), H2O2 (MESH:D006861), 16-O-methylcafestol (MESH:C000600293), cafestol (MESH:C053400)
- **Species:** Coffea arabica (arabica coffee, species) [taxon 13443], Coffea canephora (robusta coffee, species) [taxon 49390], Trichophyton rubrum (species) [taxon 5551], Coffea (coffee, genus) [taxon 13442], Mus musculus (house mouse, species) [taxon 10090], Caenorhabditis elegans (species) [taxon 6239], Pichia kudriavzevii (species) [taxon 4909], Coffea pseudozanguebariae (species) [taxon 49376], Rodentia (rodent, order) [taxon 9989], Staphylococcus epidermidis (species) [taxon 1282], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Staphylococcus aureus (species) [taxon 1280], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Lodderomyces parapsilosis (species) [taxon 5480], Trichophyton mentagrophytes (species) [taxon 523103]
- **Cell lines:** RAW 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493), B16F10 — Mus musculus (Mouse), Mouse melanoma, Cancer cell line (CVCL_0159), L929 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_AR58), BJ — Homo sapiens (Human), Telomerase immortalized cell line (CVCL_6573), RAW 267.2 — Mus musculus (Mouse), Hybridoma (CVCL_LN02), HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038), Hs68 — Homo sapiens (Human), Canavan disease, Finite cell line (CVCL_0839)

## Full text

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## Figures

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## References

81 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938085/full.md

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Source: https://tomesphere.com/paper/PMC12938085