TY - JOUR
T1 - Targeting Alpha7 Nicotinic Acetylcholine Receptors in Lung Cancer
T2 - Insights, Challenges, and Therapeutic Strategies
AU - Arunrungvichian, Kuntarat
AU - Vajragupta, Opa
AU - Hayakawa, Yoshihiro
AU - Pongrakhananon, Varisa
N1 - Publisher Copyright:
© 2023 American Chemical Society
PY - 2024/1/12
Y1 - 2024/1/12
N2 - Alpha7 nicotinic acetylcholine receptor (α7 nAChR) is an ion-gated calcium channel that plays a significant role in various aspects of cancer pathogenesis, particularly in lung cancer. Preclinical studies have elucidated the molecular mechanism underlying α7 nAChR-associated lung cancer proliferation, chemotherapy resistance, and metastasis. Understanding and targeting this mechanism are crucial for developing therapeutic interventions aimed at disrupting α7 nAChR-mediated cancer progression and improving treatment outcomes. Drug research and discovery have determined natural compounds and synthesized chemical antagonists that specifically target α7 nAChR. However, approved α7 nAChR antagonists for clinical use are lacking, primarily due to challenges related to achieving the desired selectivity, efficacy, and safety profiles required for effective therapeutic intervention. This comprehensive review provided insights into the molecular mechanisms associated with α7 nAChR and its role in cancer progression, particularly in lung cancer. Furthermore, it presents an update on recent evidence about α7 nAChR antagonists and addresses the challenges encountered in drug research and discovery in this field.
AB - Alpha7 nicotinic acetylcholine receptor (α7 nAChR) is an ion-gated calcium channel that plays a significant role in various aspects of cancer pathogenesis, particularly in lung cancer. Preclinical studies have elucidated the molecular mechanism underlying α7 nAChR-associated lung cancer proliferation, chemotherapy resistance, and metastasis. Understanding and targeting this mechanism are crucial for developing therapeutic interventions aimed at disrupting α7 nAChR-mediated cancer progression and improving treatment outcomes. Drug research and discovery have determined natural compounds and synthesized chemical antagonists that specifically target α7 nAChR. However, approved α7 nAChR antagonists for clinical use are lacking, primarily due to challenges related to achieving the desired selectivity, efficacy, and safety profiles required for effective therapeutic intervention. This comprehensive review provided insights into the molecular mechanisms associated with α7 nAChR and its role in cancer progression, particularly in lung cancer. Furthermore, it presents an update on recent evidence about α7 nAChR antagonists and addresses the challenges encountered in drug research and discovery in this field.
KW - antagonist
KW - cancer progression
KW - lung cancer
KW - α7 nAChR
UR - http://www.scopus.com/inward/record.url?scp=85181050499&partnerID=8YFLogxK
U2 - 10.1021/acsptsci.3c00138
DO - 10.1021/acsptsci.3c00138
M3 - 総説
C2 - 38230275
AN - SCOPUS:85181050499
SN - 2575-9108
VL - 7
SP - 28
EP - 41
JO - ACS Pharmacology and Translational Science
JF - ACS Pharmacology and Translational Science
IS - 1
ER -