Sains Malaysiana 52(2)(2023): 441-465
http://doi.org/10.17576/jsm-2023-5202-10
Artocarpus heterophyllus Lam. Stem Bark
Inhibits Melanogenesis through Regulation of ROS, cAMP, and MAPK Pathways
(Artocarpus heterophyllus Lam. Kulit Batang Merencat Melanogenesis melalui Pengawalaturan Laluan ROS, cAMP dan MAPK)
HAZWANI
MAT SAAD1, CHUN HOE TAN2, SUGUMARAN MANICKAM3,
SIEW HUAH LIM4 & KAE SHIN SIM1,*
1Institute
of Biological Sciences, Faculty of Science, Universiti Malaya, Jalan Profesor Diraja Ungku Aziz, 50603 Kuala Lumpur, Federal Territory,
Malaysia
2Department
of Biotechnology, Faculty of Applied Science, Lincoln University, 47301 Petaling Jaya, Selangor Darul Ehsan, Malaysia
3Rimba Ilmu Botanical Garden, UM Sustainability Development
Centre, Level 6, Research and Innovation Management Complex, Universiti Malaya, Jalan Profesor Diraja Ungku Aziz, 50603
Kuala Lumpur, Federal Territory, Malaysia
4Department
of Chemistry, Faculty of Science, Universiti Malaya,
Jalan Profesor Diraja Ungku Aziz, 50603 Kuala Lumpur, Federal Territory, Malaysia
Received:
17 August 2022/Accepted: 23 November 2022
Abstract
Natural-based skin-lightening cosmeceutical products are
attracting high popularity nowadays due to their relatively high
bioavailability upon application. Artocarpus species have been highlighted with such potential, and our previous studies
have reported that Artocarpus heterophyllusLam. stem bark extract exhibited a potent
anti-melanogenic activity by reducing melanin content and inhibiting cellular tyrosinase
activity in B16F10 melanoma cells. Hence, this study
aimed to identify
the bioactive fraction from A. heterophyllus Lam. stem bark and determine its anti-melanogenic mechanisms in B16F10 melanoma
cells. Our
results showed that a fraction (H-3) demonstrated the most pronounced
anti-melanogenic effect at 12.00 µg/mL by reducing melanin content to 22.86 ±
2.90% and inhibiting cellular
tyrosinase activity at treatment concentration 33-fold lower than kojic acid, without being cytotoxic against B16F10 melanoma cells.
Moreover, treatment with H-3 for 24 and 48 h substantially scavenged
intracellular reactive oxygen species (ROS) of hydrogen peroxide-challenged
B16F10 melanoma cells by 1.8 and 4.4%,
respectively. Based on the microarray profiling and qPCR analysis, H-3
downregulated Creb3l1, Creb3l2, Creb3l3, Mitf, Tyr, Tyrp1, and Dct genes in B16F10 melanoma cells, whereas
the expression of Map3k20, Mapk14 (p38), and Foxo3 genes was markedly
increased. Altogether, these results demonstrated that H-3 exhibited its
anti-melanogenic activity in B16F10 melanoma cells through scavenging ROS and
concurrent inhibition of the cAMP and activation of the p38/MAPK signaling pathways. These
findings indicate that H-3 has the potential to be used as a skin lightening
cosmeceutical agent in the treatment of skin hyperpigmentation.
Keywords: B16F10 melanoma cells; melanin; microarray profiling; microphthalmia-associated
transcription factor; tyrosinase
Abstrak
Produk kosmetik
pencerah kulit berasaskan sumber semula jadi mempunyai kepopularan yang tinggi
pada masa kini kerana bioketersediaannya yang tinggi apabila digunakan. Spesies Artocarpus telah diserlahkan dengan potensi sedemikian dan kajian kami
yang terdahulu telah melaporkan bahawa ekstrak kulit batang Artocarpus heterophyllus Lam. menunjukkan aktiviti anti-melanogenik yang kuat dengan menurunkan
kandungan melanin serta menghalang aktiviti tirosinase sel pada sel melanoma
B16F10. Oleh itu, kajian ini bertujuan untuk mengenal pasti
fraksi bioaktif daripada kulit batang A. heterophyllus Lam. dan
menentukan mekanisme anti-melanogenesis dalam sel melanoma B16F10. Hasil menunjukkan bahawa fraksi H-3
menunjukkan kesan anti-melanogenik yang ketara pada 12.00 µg/mL dengan
menurunkan kandungan melanin kepada 22.86 ± 2.90% serta menghalang aktiviti
tirosinase sel pada kepekatan 33 kali ganda lebih rendah berbanding asid kojik
tanpa kesan ketoksikan pada sel melanoma B16F10. Tambahan pula, rawatan dengan
H-3 selama 24 dan 48 jam dapat menghapuskan spesies oksigen reaktif (ROS)
intrasel daripada sel melanoma B16F10 yang dicabar dengan H2O2 dengan ketara masing-masing sebanyak 1.8 dan 4.4%. Berdasarkan profil jujukan
mikroarai dan analisis qPCR, H-3 menurunkan pengekspresan gen Creb3l1,
Creb3l2, Creb3l3, Mitf, Tyr, Tyrp1 dan Dct dalam
sel B16F10, manakala pengekspresan gen Map3k20, Mapk14 (p38), dan Foxo3 telah meningkat dengan ketara. Secara amnya, keputusan ini
menunjukkan bahawa H-3 menunjukkan aktiviti anti-melanogenesis dalam sel
melanoma B16F10 dengan mengikis ROS intrasel dan pada masa yang sama menghalang
laluan isyarat cAMP serta mengaktifkan isyarat laluan p38/MAPK. Penemuan ini
menunjukkan bahawa H-3 berpotensi untuk digunakan sebagai agen kosmetik
pencerah kulit dalam rawatan hiperpigmentasi kulit.
Kata kunci: Faktor
transkripsi berkaitan mikroftalmia; melanin; profil mikroatur; sel melanoma
B16F10; tirosinase
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*Corresponding author; email:
simkaeshin@um.edu.my
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