A Comparative Study of Melittins from Apis florea and Apis mellifera as Cytotoxic Agents Against Non-Small Cell Lung Cancer (NSCLC) Cells and Their Combination with Gefitinib

被引:0
作者
Sattayawat, Pachara [1 ,2 ,3 ]
Kaewkod, Thida [1 ,2 ,3 ]
Thongyim, Saruda [1 ,2 ,4 ]
Chiawpanit, Chutipa [1 ,2 ,4 ]
Wutti-in, Yupanun [2 ,5 ]
Thepmalee, Chutamas [6 ]
Tragoolpua, Yingmanee [1 ,2 ,3 ]
Disayathanoowat, Terd [1 ,3 ]
Panya, Aussara [1 ,2 ,3 ]
机构
[1] Chiang Mai Univ, Fac Sci, Dept Biol, Chiang Mai 50200, Thailand
[2] Chiang Mai Univ, Fac Sci, Cell Engn Canc Therapy Res Grp, Chiang Mai 50200, Thailand
[3] Chiang Mai Univ, Fac Sci, Res Ctr Deep Technol Beekeeping & Bee Prod Sustain, Chiang Mai 50200, Thailand
[4] Chiang Mai Univ, Off Res Adm, Chiang Mai 50200, Thailand
[5] Chiang Mai Univ, Fac Associated Med Sci, Dept Med Technol, Chiang Mai 50200, Thailand
[6] Univ Phayao, Sch Med Sci, Div Biochem, Phayao 56000, Thailand
关键词
anti-cancer peptides; melittin; NSCLC; bee venom; EGFR; EGFR MUTATION; RESISTANCE; INHIBITION; INVASION; LINES;
D O I
10.3390/ijms26062498
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lung cancer remains one of the most lethal malignancies, often diagnosed at advanced stages, leading to limited treatment options. Thus, identifying natural products with potent anti-cancer activity is crucial for improving treatment outcomes. While the melittin from Apis mellifera (Mel-AM) has been extensively studied, the melittin from Apis florea (Mel-AF), a bee species native to Southeast Asia, remains relatively underexplored. These peptides were comparatively investigated against non-small cell lung cancer (NSCLC) cell lines, A549, NCI-H460, and NCI-H1975. Mel-AF demonstrated a superior cytotoxicity (cytotoxic concentration 50% (CC50) = 2.55-5.06 mu g/mL) compared to Mel-AM (CC50 = 4.32-8.48 mu g/mL). While both peptides induced apoptosis via the intrinsic mitochondrial pathway, Mel-AF exhibited a more pronounced effect, significantly enhancing apoptosis induction compared to Mel-AM. Both peptides inhibited cell migration and invasion; however, when combined with gefitinib, Mel-AF more effectively enhanced the drug's inhibitory effects on the A549 and NCI-H460 cell lines compared to Mel-AM, underscoring its superior potential as a therapeutic agent. Altogether, we demonstrated that these peptides induced apoptosis in NSCLC cell lines, with Mel-AF having more pronounced effects, and the combination use of peptides with a chemotherapeutic drug showed synergistic effects against lung cancer cells, enhancing their practical use in lung cancer treatments.
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页数:19
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