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P. 311

FR-04


               Bletilla  formosana  and  its  constituents  as  promising  therapeutics  via

               modulation of redox homeostasis in colorectal cancer


                                                                          3
                                                       #,2
                                  #,1
               Sheng-Chieh Tsai,  Chun-Hong Chen,  Y u -Chia Chang,  Po-Jen Chen*         ,1,2

               1  Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University,
                 Kaohsiung 807378, Taiwan
               2  Department of Pharmacology, School of Medicine, College of Medicine, Kaohsiung
                 Medical University, Kaohsiung 807378, Taiwan
               3  Center for Drug Research and Development and Graduate Institute of Health Industry
                 Technology, College of Human Ecology, Chang Gung University of Science and
                 Technology, Taoyuan 333324, Taiwan
               * E-mail: pjc@kmu.edu.tw

               Abstract
                  Cancer is the leading cause of death in Taiwan, with colorectal cancer (CRC) consistently
               ranking among the top in terms of incidence and mortality. Bletilla formosana (Hayata) Schltr,
               a Taiwan native herbal medicine, is traditionally utilized to manage bleeding and inflammation;
               however, current research into its anticancer properties and mechanisms remains limited. Using
               bioactivity-directed  fractionation  strategy  combined  with  chemical  molecular  networking
               analysis,  we  ideintified  that  the  primary  anticancer  constituents  of  B.  formosana  were
               concentrated  within  its  ethyl  acetate  (EA)  extract,  primarily  consisting  of  benzyl  and
               phenanthrene  natural  products. The  EA  extract  potentially  exerted  its  anticancer  effects  by
               inducing mitophagy-mediated mitochondrial dysfunction and redox stress, ultimately leading
               to apoptosis in CRC cells. In vivo studies using mouse models confirmed the efficacy of the
               benzyl  natural  product  in  inhibiting  CRC  cell  growth.  These  findings  provide  promising
               evidence  for  B.  formosana  and  its  constituents  as  novel  anticancer  therapeutic  agents  via
               modulation of redox homeostasis.

               Keywords: B. formosana; Colorectal cancer; Redox homeostasis; Mitochondrial damage
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