Cargando…

Oral intake of royal jelly improves anti-cancer effects and suppresses adverse events of molecular targeted therapy by regulating TNF-α and TGF-β in renal cell carcinoma: A preliminary study based on a randomized double-blind clinical trial

Molecular targeted therapies are commonly used in patients with metastatic renal cell carcinoma (RCC). However, the efficacy and safety of these therapeutic interventions require enhancement to improve prognosis in these patients. Royal jelly (RJ) has anti-cancer effects and adverse events across a...

Descripción completa

Detalles Bibliográficos
Autores principales: Miyata, Yasuyoshi, Araki, Kyohei, Ohba, Kojiro, Mastuo, Tomhiro, Nakamura, Yuichiro, Yuno, Tsutomu, Mukai, Yuta, Otsubo, Asato, Mitsunari, Kensuke, Mochizuki, Yasushi, Sakai, Hideki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403815/
https://www.ncbi.nlm.nih.gov/pubmed/32765876
http://dx.doi.org/10.3892/mco.2020.2099
_version_ 1783567015454179328
author Miyata, Yasuyoshi
Araki, Kyohei
Ohba, Kojiro
Mastuo, Tomhiro
Nakamura, Yuichiro
Yuno, Tsutomu
Mukai, Yuta
Otsubo, Asato
Mitsunari, Kensuke
Mochizuki, Yasushi
Sakai, Hideki
author_facet Miyata, Yasuyoshi
Araki, Kyohei
Ohba, Kojiro
Mastuo, Tomhiro
Nakamura, Yuichiro
Yuno, Tsutomu
Mukai, Yuta
Otsubo, Asato
Mitsunari, Kensuke
Mochizuki, Yasushi
Sakai, Hideki
author_sort Miyata, Yasuyoshi
collection PubMed
description Molecular targeted therapies are commonly used in patients with metastatic renal cell carcinoma (RCC). However, the efficacy and safety of these therapeutic interventions require enhancement to improve prognosis in these patients. Royal jelly (RJ) has anti-cancer effects and adverse events across a variety of types of malignancy. The present study investigated the detailed mechanism underlying the effects of oral administration of RJ in patients with advanced RCC that were treated with molecular targeted agents in a randomized clinical trial. The study cohort comprised 16 patients treated with RJ and 17 patients treated with a placebo. Serum levels of tumor necrosis factor (TNF)-α and transforming growth factor (TGF)-β were measured using enzyme-linked immunosorbent assays. The results of the present study demonstrated a larger decrease in tumor size upon supplementing patients with RJ following molecular targeted therapy compared with that in patients administered with the placebo. Patients exhibited reduced anorexia and fatigue in the RJ group compared with the placebo group. The relative dose intensity for patients in the RJ group was higher than that in patients in the placebo group. Post- and pre-treatment ratios of the serum levels of TNF-α and TGF-β in patients in the RJ group were lower than those in patients in the placebo group, and these ratios correlated with decreasing tumor size and frequency of anorexia or fatigue in patients. In conclusion, the results of the present study indicated that oral intake of RJ improved the efficacy and safety of molecular targeted therapy in patients with RCC and changed the levels of TNF-α and TGF-β in the serum of patients, which is speculated to serve an important role in RJ-induced biological activities.
format Online
Article
Text
id pubmed-7403815
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-74038152020-08-05 Oral intake of royal jelly improves anti-cancer effects and suppresses adverse events of molecular targeted therapy by regulating TNF-α and TGF-β in renal cell carcinoma: A preliminary study based on a randomized double-blind clinical trial Miyata, Yasuyoshi Araki, Kyohei Ohba, Kojiro Mastuo, Tomhiro Nakamura, Yuichiro Yuno, Tsutomu Mukai, Yuta Otsubo, Asato Mitsunari, Kensuke Mochizuki, Yasushi Sakai, Hideki Mol Clin Oncol Articles Molecular targeted therapies are commonly used in patients with metastatic renal cell carcinoma (RCC). However, the efficacy and safety of these therapeutic interventions require enhancement to improve prognosis in these patients. Royal jelly (RJ) has anti-cancer effects and adverse events across a variety of types of malignancy. The present study investigated the detailed mechanism underlying the effects of oral administration of RJ in patients with advanced RCC that were treated with molecular targeted agents in a randomized clinical trial. The study cohort comprised 16 patients treated with RJ and 17 patients treated with a placebo. Serum levels of tumor necrosis factor (TNF)-α and transforming growth factor (TGF)-β were measured using enzyme-linked immunosorbent assays. The results of the present study demonstrated a larger decrease in tumor size upon supplementing patients with RJ following molecular targeted therapy compared with that in patients administered with the placebo. Patients exhibited reduced anorexia and fatigue in the RJ group compared with the placebo group. The relative dose intensity for patients in the RJ group was higher than that in patients in the placebo group. Post- and pre-treatment ratios of the serum levels of TNF-α and TGF-β in patients in the RJ group were lower than those in patients in the placebo group, and these ratios correlated with decreasing tumor size and frequency of anorexia or fatigue in patients. In conclusion, the results of the present study indicated that oral intake of RJ improved the efficacy and safety of molecular targeted therapy in patients with RCC and changed the levels of TNF-α and TGF-β in the serum of patients, which is speculated to serve an important role in RJ-induced biological activities. D.A. Spandidos 2020-10 2020-07-20 /pmc/articles/PMC7403815/ /pubmed/32765876 http://dx.doi.org/10.3892/mco.2020.2099 Text en Copyright: © Miyata et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Miyata, Yasuyoshi
Araki, Kyohei
Ohba, Kojiro
Mastuo, Tomhiro
Nakamura, Yuichiro
Yuno, Tsutomu
Mukai, Yuta
Otsubo, Asato
Mitsunari, Kensuke
Mochizuki, Yasushi
Sakai, Hideki
Oral intake of royal jelly improves anti-cancer effects and suppresses adverse events of molecular targeted therapy by regulating TNF-α and TGF-β in renal cell carcinoma: A preliminary study based on a randomized double-blind clinical trial
title Oral intake of royal jelly improves anti-cancer effects and suppresses adverse events of molecular targeted therapy by regulating TNF-α and TGF-β in renal cell carcinoma: A preliminary study based on a randomized double-blind clinical trial
title_full Oral intake of royal jelly improves anti-cancer effects and suppresses adverse events of molecular targeted therapy by regulating TNF-α and TGF-β in renal cell carcinoma: A preliminary study based on a randomized double-blind clinical trial
title_fullStr Oral intake of royal jelly improves anti-cancer effects and suppresses adverse events of molecular targeted therapy by regulating TNF-α and TGF-β in renal cell carcinoma: A preliminary study based on a randomized double-blind clinical trial
title_full_unstemmed Oral intake of royal jelly improves anti-cancer effects and suppresses adverse events of molecular targeted therapy by regulating TNF-α and TGF-β in renal cell carcinoma: A preliminary study based on a randomized double-blind clinical trial
title_short Oral intake of royal jelly improves anti-cancer effects and suppresses adverse events of molecular targeted therapy by regulating TNF-α and TGF-β in renal cell carcinoma: A preliminary study based on a randomized double-blind clinical trial
title_sort oral intake of royal jelly improves anti-cancer effects and suppresses adverse events of molecular targeted therapy by regulating tnf-α and tgf-β in renal cell carcinoma: a preliminary study based on a randomized double-blind clinical trial
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403815/
https://www.ncbi.nlm.nih.gov/pubmed/32765876
http://dx.doi.org/10.3892/mco.2020.2099
work_keys_str_mv AT miyatayasuyoshi oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial
AT arakikyohei oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial
AT ohbakojiro oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial
AT mastuotomhiro oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial
AT nakamurayuichiro oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial
AT yunotsutomu oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial
AT mukaiyuta oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial
AT otsuboasato oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial
AT mitsunarikensuke oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial
AT mochizukiyasushi oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial
AT sakaihideki oralintakeofroyaljellyimprovesanticancereffectsandsuppressesadverseeventsofmoleculartargetedtherapybyregulatingtnfaandtgfbinrenalcellcarcinomaapreliminarystudybasedonarandomizeddoubleblindclinicaltrial