Natural Compound Allicin Containing Thiosulfinate Moieties as Transmembrane Protein 16A (TMEM16A) Ion Channel Inhibitor for Food Adjuvant Therapy of Lung Cancer.

Cancer is one of the most serious malignant diseases, and chemotherapy is cancer's main clinical treatment method. However, chemotherapy inevitably produces drug resistance, and side effects accompany them. Adjuvant therapy is an effective way to enhance chemotherapeutic drug sensitivity and reduce side effects. This study found allicin, garlic's active ingredient, is an inhibitor of transmembrane protein 16A (TMEM16A), a novel drug target of lung adenocarcinoma. Allicin concentration-dependently inhibited TMEM16A currents with an IC50 of 24.35 ± 4.14 μM. Allicin thiosulfinate moieties bound with R535A/E624A/E633A residues of TMEM16A blocked the ion transport function and downregulated TMEM16A protein expression affecting the mitogen-activated protein kinase signal transduction. Then, allicin reduced the viability and migration of LA795 cells, and induced cell apoptosis. Moreover, multitarget combination administration results indicated that the therapeutic effect of 3.56 mg/kg allicin and 3 mg/kg cisplatin combined administration was superior to the superposition of the two drugs alone, demonstrating that the anticancer effects of allicin and cisplatin were synergistic. In addition, low-concentration combined administration also avoided the side effects of cisplatin in mice. Based on the good tumor suppressor effect and high biosafety of allicin and cisplatin combination in vivo, allicin can be used for food adjuvant therapy of cisplatin chemotherapy.

[1]  Caicun Zhou,et al.  Non‐small cell lung cancer in China , 2022, Cancer communications.

[2]  Libo He,et al.  Systematic assessment of microRNAs associated with lung cancer and physical exercise , 2022, Frontiers in Oncology.

[3]  Jin-Kyoung Oh,et al.  Smoking trajectory and cancer risk: A population-based cohort study , 2022, Tobacco induced diseases.

[4]  Wei Cheng,et al.  The modulation of ion channels in cancer chemo-resistance , 2022, Frontiers in Oncology.

[5]  Hongzan Song,et al.  Self-healing pectin/cellulose hydrogel loaded with limonin as TMEM16A inhibitor for lung adenocarcinoma treatment. , 2022, International journal of biological macromolecules.

[6]  Wenjie Zhong,et al.  Targeted Therapy in Early Stage Non-small Cell Lung Cancer , 2022, Current Treatment Options in Oncology.

[7]  Hailong An,et al.  Multi-target tracheloside and doxorubicin combined treatment of lung adenocarcinoma. , 2022, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[8]  Hailong An,et al.  Caffeic Acid, an Active Ingredient in Coffee, Combines with DOX for Multitarget Combination Therapy of Lung Cancer. , 2022, Journal of agricultural and food chemistry.

[9]  S. Yanamoto,et al.  TMEM16A as a potential treatment target for head and neck cancer , 2022, Journal of experimental & clinical cancer research : CR.

[10]  Dingsheng Zhao,et al.  Anoctamin 1 controls bone resorption by coupling Cl− channel activation with RANKL-RANK signaling transduction , 2022, Nature Communications.

[11]  N. Khalili,et al.  Tumor-infiltrating lymphocyte therapy for lung cancer and its future paradigms , 2022, Expert opinion on biological therapy.

[12]  Hailong An,et al.  Nuciferine Inhibits TMEM16A in Dietary Adjuvant Therapy for Lung Cancer. , 2022, Journal of agricultural and food chemistry.

[13]  Liegang Liu,et al.  Current studies and potential future research directions on biological effects and related mechanisms of allicin , 2022, Critical reviews in food science and nutrition.

[14]  J. Hong,et al.  Chloride Channels and Transporters: Roles beyond Classical Cellular Homeostatic pH or Ion Balance in Cancers , 2022, Cancers.

[15]  A. Asadi,et al.  Effect of astaxanthin and melatonin on cell viability and DNA damage in human breast cancer cell lines. , 2021, Acta histochemica.

[16]  B. Mahdi,et al.  Development of topical patches releasing allicin using garlic extract , 2021, Journal of cosmetic dermatology.

[17]  Hailong An,et al.  TMEM16A, a Homoharringtonine Receptor, as a Potential Endogenic Target for Lung Cancer Treatment , 2021, International journal of molecular sciences.

[18]  Hailong An,et al.  Emerging Modulators of TMEM16A and Their Therapeutic Potential , 2021, The Journal of Membrane Biology.

[19]  M. Waly,et al.  Ketogenic Diet in Cancer Prevention and Therapy: Molecular Targets and Therapeutic Opportunities , 2021, Current issues in molecular biology.

[20]  Y. Kamisah,et al.  New Insights into Molecular Mechanism behind Anti-Cancer Activities of Lycopene , 2021, Molecules.

[21]  S. Hsia,et al.  Fish Oil, Se Yeast, and Micronutrient-Enriched Nutrition as Adjuvant Treatment during Target Therapy in a Murine Model of Lung Cancer , 2021, Marine drugs.

[22]  Shuai Guo,et al.  Inhibition of TMEM16A by Natural Product Silibinin: Potential Lead Compounds for Treatment of Lung Adenocarcinoma , 2021, Frontiers in Pharmacology.

[23]  R. Pazdur,et al.  Contribution of Early Clinical Benefit End Points to Decreased Lung Cancer Mortality Rates. , 2021, JAMA oncology.

[24]  Xiaoli Xie,et al.  The Prognostic Value and Mechanisms of TMEM16A in Human Cancer , 2021, Frontiers in Molecular Biosciences.

[25]  A. Jemal,et al.  Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries , 2021, CA: a cancer journal for clinicians.

[26]  Youwen Zhong,et al.  Enhancer of mRNA Decapping protein 4 (EDC4) interacts with replication protein a (RPA) and contributes to Cisplatin resistance in cervical Cancer by alleviating DNA damage , 2020, Hereditas.

[27]  J. Cui,et al.  TMEM16A-inhibitor loaded pH-responsive nanoparticles: a novel dual-targeting antitumor therapy for lung adenocarcinoma. , 2020, Biochemical pharmacology.

[28]  Hailin Zhang,et al.  Arctigenin, a novel TMEM16A inhibitor for lung adenocarcinoma therapy. , 2020, Pharmacological research.

[29]  Hailong An,et al.  The Molecular Mechanism of Ginsenoside Analogs Activating TMEM16A. , 2019, Biophysical journal.

[30]  Jinlong Qi,et al.  Entering the spotlight: Chitosan oligosaccharides as novel activators of CaCCs/TMEM16A. , 2019, Pharmacological research.

[31]  C. Song,et al.  A mutual activation loop between the Ca2+-activated chloride channel TMEM16A and EGFR/STAT3 signaling promotes breast cancer tumorigenesis. , 2019, Cancer letters.

[32]  L. Jan,et al.  The multifaceted role of TMEM16A in cancer. , 2019, Cell calcium.

[33]  Y. Jan,et al.  TMEM16A controls EGF-induced calcium signaling implicated in pancreatic cancer prognosis , 2019, Proceedings of the National Academy of Sciences.

[34]  S. Ghavamzadeh,et al.  Curcumin and Gastric Cancer: a Review on Mechanisms of Action , 2019, Journal of Gastrointestinal Cancer.

[35]  Liana C. Silva,et al.  Cisplatin-Membrane Interactions and Their Influence on Platinum Complexes Activity and Toxicity , 2019, Front. Physiol..

[36]  Hailong An,et al.  Recent advances in TMEM16A: Structure, function, and disease , 2018, Journal of cellular physiology.

[37]  Hailong An,et al.  Matrine is a novel inhibitor of the TMEM16A chloride channel with antilung adenocarcinoma effects , 2018, Journal of cellular physiology.

[38]  A. Rahmani,et al.  Ginger: A Novel Strategy to Battle Cancer through Modulating Cell Signalling Pathways: A Review. , 2019, Current pharmaceutical biotechnology.

[39]  J. Lang,et al.  Potential protective role of hydrogen against cisplatininduced side effects during chemotherapy: A mini-review of a novel hypothesis for antagonism of hydrogen , 2018 .

[40]  M. Wei,et al.  Cell-specific mechanisms of TMEM16A Ca2+-activated chloride channel in cancer , 2017, Molecular Cancer.

[41]  Olivier Michielin,et al.  SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules , 2017, Scientific Reports.

[42]  Hailin Zhang,et al.  Ginsenoside Rb1, a novel activator of the TMEM16A chloride channel, augments the contraction of guinea pig ileum , 2017, Pflügers Archiv - European Journal of Physiology.

[43]  E. Hwang,et al.  Surface expression of the Anoctamin-1 (ANO1) channel is suppressed by protein-protein interactions with β-COP. , 2016, Biochemical and biophysical research communications.

[44]  Yin-gang Ren,et al.  Transmembrane protein with unknown function 16A overexpression promotes glioma formation through the nuclear factor-κB signaling pathway. , 2014, Molecular medicine reports.

[45]  H. C. Hartzell,et al.  Anoctamin 1 (Tmem16A) Ca2+-activated chloride channel stoichiometrically interacts with an ezrin–radixin–moesin network , 2012, Proceedings of the National Academy of Sciences.

[46]  Ting-Chao Chou,et al.  Theoretical Basis, Experimental Design, and Computerized Simulation of Synergism and Antagonism in Drug Combination Studies , 2006, Pharmacological Reviews.

[47]  M. Carvajal,et al.  Chemical and biological characterisation of nutraceutical compounds of broccoli. , 2006, Journal of pharmaceutical and biomedical analysis.