9 research outputs found
Nutraceuticals and Exercise against Muscle Wasting during Cancer Cachexia
- Publication venue
- 'MDPI AG'
- Publication date
- 09/12/2020
- Field of study
Cancer cachexia (CC) is a debilitating multifactorial syndrome, involving progressive deterioration and functional impairment of skeletal muscles. It affects about 80% of patients with advanced cancer and causes premature death. No causal therapy is available against CC. In the last few decades, our understanding of the mechanisms contributing to muscle wasting during cancer has markedly increased. Both inflammation and oxidative stress (OS) alter anabolic and catabolic signaling pathways mostly culminating with muscle depletion. Several preclinical studies have emphasized the beneficial roles of several classes of nutraceuticals and modes of physical exercise, but their efficacy in CC patients remains scant. The route of nutraceutical administration is critical to increase its bioavailability and achieve the desired anti-cachexia effects. Accumulating evidence suggests that a single therapy may not be enough, and a bimodal intervention (nutraceuticals plus exercise) may be a more effective treatment for CC. This review focuses on the current state of the field on the role of inflammation and OS in the pathogenesis of muscle atrophy during CC, and how nutraceuticals and physical activity may act synergistically to limit muscle wasting and dysfunction
Costameric integrin and sarcoglycan protein levels are altered in a Drosophila model for Limb-girdle muscular dystrophy type 2H
- Author
- Publication venue
- 'American Society for Cell Biology (ASCB)'
- Publication date
- 05/01/2022
- Field of study
Mutations in two different domains of the ubiquitously expressed TRIM32 protein give rise to two clinically separate diseases, one of which is Limb-girdle muscular dystrophy type 2H (LGMD2H). Uncovering the muscle-specific role of TRIM32 in LGMD2H pathogenesis has proven difficult, as neurogenic phenotypes, independent of LGMD2H pathology, are present in TRIM32 KO mice. We previously established a platform to study LGMD2H pathogenesis using Drosophila melanogaster as a model. Here we show that LGMD2H disease-causing mutations in the NHL domain are molecularly and structurally conserved between fly and human TRIM32. Furthermore, transgenic expression of a subset of myopathic alleles (R394H, D487N, and 520fs) induce myofibril abnormalities, altered nuclear morphology, and reduced TRIM32 protein levels, mimicking phenotypes in patients afflicted with LGMD2H. Intriguingly, we also report for the first time that the protein levels of βPS integrin and sarcoglycan δ, both core components of costameres, are elevated in TRIM32 disease-causing alleles. Similarly, murine myoblasts overexpressing a catalytically inactive TRIM32 mutant aberrantly accumulate α- and β-dystroglycan and α-sarcoglycan. We speculate that the stoichiometric loss of costamere components disrupts costamere complexes to promote muscle degeneration
Nutraceuticals and Exercise against Muscle Wasting during Cancer Cachexia
- Publication venue
- 'MDPI AG'
- Publication date
- 24/11/2020
- Field of study
Cancer cachexia (CC) is a debilitating multifactorial syndrome, involving progressive deterioration and functional impairment of skeletal muscles. It affects about 80% of patients with advanced cancer and causes premature death. No causal therapy is available against CC. In the last few decades, our understanding of the mechanisms contributing to muscle wasting during cancer has markedly increased. Both inflammation and oxidative stress (OS) alter anabolic and catabolic signaling pathways mostly culminating with muscle depletion. Several preclinical studies have emphasized the beneficial roles of several classes of nutraceuticals and modes of physical exercise, but their efficacy in CC patients remains scant. The route of nutraceutical administration is critical to increase its bioavailability and achieve the desired anti-cachexia effects. Accumulating evidence suggests that a single therapy may not be enough, and a bimodal intervention (nutraceuticals plus exercise) may be a more effective treatment for CC. This review focuses on the current state of the field on the role of inflammation and OS in the pathogenesis of muscle atrophy during CC, and how nutraceuticals and physical activity may act synergistically to limit muscle wasting and dysfunction
Group I Paks support muscle regeneration and counteract cancer‐associated muscle atrophy
- Author
- Publication venue
- 'Wiley'
- Publication date
- 01/08/2018
- Field of study
Abstract Background Skeletal muscle is characterized by an efficient regeneration potential that is often impaired during myopathies. Understanding the molecular players involved in muscle homeostasis and regeneration could help to find new therapies against muscle degenerative disorders. Previous studies revealed that the Ser/Thr kinase p21 protein‐activated kinase 1 (Pak1) was specifically down‐regulated in the atrophying gastrocnemius of Yoshida hepatoma‐bearing rats. In this study, we evaluated the role of group I Paks during cancer‐related atrophy and muscle regeneration. Methods We examined Pak1 expression levels in the mouse Tibialis Anterior muscles during cancer cachexia induced by grafting colon adenocarcinoma C26 cells and in vitro by dexamethasone treatment. We investigated whether the overexpression of Pak1 counteracts muscle wasting in C26‐bearing mice and in vitro also during interleukin‐6 (IL6)‐induced or dexamethasone‐induced C2C12 atrophy. Moreover, we analysed the involvement of group I Paks on myogenic differentiation in vivo and in vitro using the group I chemical inhibitor IPA‐3. Results We found that Pak1 expression levels are reduced during cancer‐induced cachexia in the Tibialis Anterior muscles of colon adenocarcinoma C26‐bearing mice and in vitro during dexamethasone‐induced myotube atrophy. Electroporation of muscles of C26‐bearing mice with plasmids directing the synthesis of PAK1 preserves fiber size in cachectic muscles by restraining the expression of atrogin‐1 and MuRF1 and possibly by inducing myogenin expression. Consistently, the overexpression of PAK1 reduces the dexamethasone‐induced expression of MuRF1 in myotubes and increases the phospho‐FOXO3/FOXO3 ratio. Interestingly, the ectopic expression of PAK1 counteracts atrophy in vitro by restraining the IL6‐Stat3 signalling pathway measured in luciferase‐based assays and by reducing rates of protein degradation in atrophying myotubes exposed to IL6. On the other hand, we observed that the inhibition of group I Paks has no effect on myotube atrophy in vitro and is associated with impaired muscle regeneration in vivo and in vitro. In fact, we found that mice treated with the group I inhibitor IPA‐3 display a delayed recovery from cardiotoxin‐induced muscle injury. This is consistent with in vitro experiments showing that IPA‐3 impairs myogenin expression and myotube formation in vessel‐associated myogenic progenitors, C2C12 myoblasts, and satellite cells. Finally, we observed that IPA‐3 reduces p38α/β phosphorylation that is required to proceed through various stages of satellite cells differentiation: activation, asymmetric division, and ultimately myotube formation. Conclusions Our data provide novel evidence that is consistent with group I Paks playing a central role in the regulation of muscle homeostasis, atrophy and myogenesis
Transforming Growth Factor-Beta Signaling in Cancer-Induced Cachexia: From Molecular Pathways to the Clinics
- Author
- Publication venue
- 'MDPI AG'
- Publication date
- 01/01/2022
- Field of study
Cachexia is a metabolic syndrome consisting of massive loss of muscle mass and function that has a severe impact on the quality of life and survival of cancer patients. Up to 20% of lung cancer patients and up to 80% of pancreatic cancer patients are diagnosed with cachexia, leading to death in 20% of them. The main drivers of cachexia are cytokines such as interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), macrophage inhibitory cytokine 1 (MIC-1/GDF15) and transforming growth factor-beta (TGF-β). Besides its double-edged role as a tumor suppressor and activator, TGF-β causes muscle loss through myostatin-based signaling, involved in the reduction in protein synthesis and enhanced protein degradation. Additionally, TGF-β induces inhibin and activin, causing weight loss and muscle depletion, while MIC-1/GDF15, a member of the TGF-β superfamily, leads to anorexia and so, indirectly, to muscle wasting, acting on the hypothalamus center. Against this background, the blockade of TGF-β is tested as a potential mechanism to revert cachexia, and antibodies against TGF-β reduced weight and muscle loss in murine models of pancreatic cancer. This article reviews the role of the TGF-β pathway and to a minor extent of other molecules including microRNA in cancer onset and progression with a special focus on their involvement in cachexia, to enlighten whether TGF-β and such other players could be potential targets for therapy
Apelin Resistance Contributes to Muscle Loss during Cancer Cachexia in Mice
- Author
- Publication venue
- MDPI AG
- Publication date
- 01/04/2022
- Field of study
Cancer cachexia consists of dramatic body weight loss with rapid muscle depletion due to imbalanced protein homeostasis. We found that the mRNA levels of apelin decrease in muscles from cachectic hepatoma-bearing rats and three mouse models of cachexia. Furthermore, apelin expression inversely correlates with MuRF1 in muscle biopsies from cancer patients. To shed light on the possible role of apelin in cachexia in vivo, we generated apelin 13 carrying all the last 13 amino acids of apelin in D isomers, ultimately extending plasma stability. Notably, apelin D-peptides alter cAMP-based signaling in vitro as the L-peptides, supporting receptor binding. In vitro apelin 13 protects myotube diameter from dexamethasone-induced atrophy, restrains rates of degradation of long-lived proteins and MuRF1 expression, but fails to protect mice from atrophy. D-apelin 13 given intraperitoneally for 13 days in colon adenocarcinoma C26-bearing mice does not reduce catabolic pathways in muscles, as it does in vitro. Puzzlingly, the levels of circulating apelin seemingly deriving from cachexia-inducing tumors, increase in murine plasma during cachexia. Muscle electroporation of a plasmid expressing its receptor APJ, unlike apelin, preserves myofiber area from C26-induced atrophy, supporting apelin resistance in vivo. Altogether, we believe that during cachexia apelin resistance occurs, contributing to muscle wasting and nullifying any possible peptide-based treatment
Trabectedin and Lurbinectedin Extend Survival of Mice Bearing C26 Colon Adenocarcinoma, without Affecting Tumor Growth or Cachexia
- Author
- Andrea David Re Cecconi
- Andrea Resovi
- Deborah Novelli
- Emilie Vénéreau
- Eugenio Scanziani
- Ezia Bello
- Giorgia Careccia
- Giorgio Aquila
- Giulia Benedetta Martinelli
- Ilaria Russo
- Laura Pasetto
- Laura Talamini
- Lidia Staszewsky
- Mara Forti
- Maurizio D\u27Incalci
- Raffaella Giavazzi
- Roberta Frapolli
- Roberto Latini
- Rosanna Piccirillo
- Serge Masson
- Simonetta Andrea Licandro
- Publication venue
- 'MDPI AG'
- Publication date
- 17/08/2020
- Field of study
Trabectedin (ET743) and lurbinectedin (PM01183) limit the production of inflammatory cytokines that are elevated during cancer cachexia. Mice carrying C26 colon adenocarcinoma display cachexia (i.e., premature death and body wasting with muscle, fat and cardiac tissue depletion), high levels of inflammatory cytokines and subsequent splenomegaly. We tested whether such drugs protected these mice from cachexia. Ten-week-old mice were inoculated with C26 cells and three days later randomized to receive intravenously vehicle or 0.05 mg/kg ET743 or 0.07 mg/kg PM01183, three times a week for three weeks. ET743 or PM01183 extended the lifespan of C26-mice by 30% or 85%, respectively, without affecting tumor growth or food intake. Within 13 days from C26 implant, both drugs did not protect fat, muscle and heart from cachexia. Since PM01183 extended the animal survival more than ET743, we analyzed PM01183 further. In tibialis anterior of C26-mice, but not in atrophying myotubes, PM01183 restrained the NF-κB/PAX7/myogenin axis, possibly reducing the pro-inflammatory milieu, and failed to limit the C/EBPβ/atrogin-1 axis. Inflammation-mediated splenomegaly of C26-mice was inhibited by PM01183 for as long as the treatment lasted, without reducing IL-6, M-CSF or IL-1β in plasma. ET743 and PM01183 extend the survival of C26-bearing mice unchanging tumor growth or cachexia but possibly restrain muscle-related inflammation and C26-induced splenomegaly
Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356
- Author
- Abdelmohsen Kotb
- Abe Akihisa
- Abedin Md Joynal
- Abeliovich Hagai
- Adachi Hiroaki
- Adams Christopher M.
- Adams Peter D.
- Adeli Khosrow
- Adhihetty Peter J.
- Adler Sharon G.
- Agam Galila
- Agarwal Rajesh
- Aghi Manish K.
- Agnello Maria
- Agostinis Patrizia
- Aguilar Patricia V.
- Aguirre-Ghiso Julio
- Airoldi Edoardo M.
- Ait-Si-Ali Slimane
- Akematsu Takahiko
- Akporiaye Emmanuel T.
- Al-Rubeai Mohamed
- Albaiceta Guillermo M.
- Albanese Chris
- Albani Diego
- Albert Matthew L.
- Aldudo Jesus
- Algül Hana
- Alirezaei Mehrdad
- Alloza Iraide
- Almasan Alexandru
- Almonte-Beceril Maylin
- Alnemri Emad S.
- Alonso Covadonga
- Altan-Bonnet Nihal
- Altieri Dario C.
- Alvarez Silvia
- Alvarez-Erviti Lydia
- Alves Sandro
- Amadoro Giuseppina
- Amano Atsuo
- Amantini Consuelo
- Ambrosio Santiago
- Amelio Ivano
- Amer Amal O.
- Amessou Mohamed
- Amon Angelika
- An Zhenyi
- Anania Frank A.
- Andersen Stig U.
- Andley Usha P.
- Andreadi Catherine K.
- Andrieu-Abadie Nathalie
- Anel Alberto
- Ann David K.
- Anoopkumar-Dukie Shailendra
- Antonioli Manuela
- Aoki Hiroshi
- Apostolova Nadezda
- Aquila Saveria
- Aquilano Katia
- Araki Koichi
- Arama Eli
- Aranda Agustin
- Araya Jun
- Arcaro Alexandre
- Arias Esperanza
- Arimoto Hirokazu
- Ariosa Aileen R.
- Armstrong Jane L.
- Arnould Thierry
- Arozena Abraham Acevedo
- Arsov Ivica
- Asanuma Katsuhiko
- Askanas Valerie
- Asselin Eric
- Atarashi Ryuichiro
- Atherton Sally S.
- Atkin Julie D.
- Attardi Laura D.
- Auberger Patrick
- Auburger Georg
- Aurelian Laure
- Autelli Riccardo
- Avagliano Laura
- Avantaggiati Maria Laura
- Avrahami Limor
- Awale Suresh
- Azad Neelam
- Bachetti Tiziana
- Backer Jonathan M.
- Bae Dong-Hun
- Bae Jae-Sung
- Bae Ok-Nam
- Bae Soo Han
- Baehrecke Eric H.
- Baek Seung-Hoon
- Baghdiguian Stephen
- Bagniewska-Zadworna Agnieszka
- Bai Hua
- Bai Jie
- Bai Xue-Yuan
- Bailly Yannick
- Balaji Kithiganahalli Narayanaswamy
- Balduini Walter
- Ballabio Andrea
- Balzan Rena
- Banerjee Rajkumar
- Bao Haijun
- Barbato Daniele Lettieri
- Barbeau Benoit
- Barrachina Maria D.
- Barreiro Esther
- Bartel Bonnie
- Bartolomé Alberto
- Bassham Diane C.
- Bassi Maria Teresa
- Bast Robert C.
- Basu Alakananda
- Batista Maria Teresa
- Batoko Henri
- Battino Maurizio
- Bauckman Kyle
- Baumgarner Bradley L.
- Bayer K. Ulrich
- Beale Rupert
- Beaulieu Jean-François
- Beck George R.
- Becker Christoph
- Beckham J. David
- Bednarski Patrick J.
- Begley Thomas J.
- Behl Christian
- Behrends Christian
- Behrens Georg M. N.
- Behrns Kevin E.
- Bejarano Eloy
- Belaid Amine
- Belleudi Francesca
- Berchem Guy
- Bergamaschi Daniele
- Bergami Matteo
- Berkhout Ben
- Berliocchi Laura
- Bernard Amélie
- Bernard Monique
- Bernassola Francesca
- Bertolotti Anne
- Bess Amanda S.
- Besteiro Sébastien
- Bettuzzi Saverio
- Bhalla Savita
- Bhattacharyya Shalmoli
- Bhutia Sujit K.
- Biagosch Caroline
- Bianchi Michele Wolfe
- Biard-Piechaczyk Martine
- Billes Viktor
- Bincoletto Claudia
- Bingol Baris
- Bird Sara W.
- Bitoun Marc
- Bjedov Ivana
- Blackstone Craig
- Blanc Lionel
- Blanco Guillermo A.
- Blomhoff Heidi Kiil
- Boada-Romero Emilio
- Boes Marianne
- Boesze-Battaglia Kathleen
- Boise Lawrence H.
- Bolino Alessandra
- Boman Andrea
- Bonaldo Paolo
- Bordi Matteo
- Bosch Jürgen
- Botana Luis M.
- Botti Joelle
- Bou German
- Bouchecareilh Marion
- Boucher Marie-Josée
- Bouché Marina
- Boulton Michael E.
- Bouret Sebastien G.
- Boya Patricia
- Boyer-Guittaut Michaël
- Bozhkov Peter V.
- Brady Nathan
- Braga Vania M. M.
- Brancolini Claudio
- Braus Gerhard H.
- Bravosan-Pedro José M.
- Brennan Lisa A.
- Bresnick Emery H.
- Brest Patrick
- Bridges Dave
- Bringer Marie-Agnès
- Brini Marisa
- Brito Glauber C.
- Brodin Bertha
- Brookes Paul S.
- Brown Eric J.
- Brown Karen
- Broxmeyer Hal E.
- Bruhat Alain
- Brum Patricia Chakur
- Brumell John H.
- Brunetti-Pierri Nicola
- Bryson-Richardson Robert J.
- Buch Shilpa
- Buchan Alastair M.
- Budak Hikmet
- Bulavin Dmitry V.
- Bultman Scott J.
- Bultynck Geert
- Bumbasirevic Vladimir
- Burelle Yan
- Burke Robert E.
- Burmeister Margit
- Bánhegyi Gábor
- Bédard Pierre-André
- Bénard Giovanni
- Böckler Stefan
- Bütikofer Peter
- Caberlotto Laura
- Cadwell Ken
- Cahova Monika
- Cai Dongsheng
- Cai Jingjing
- Cai Qian
- Calatayud Sara
- Camougrand Nadine
- Campagne Menno van Lookeren
- Campanella Michelangelo
- Campbell Grant R.
- Campbell Matthew
- Campello Silvia
- Candau Robin
- Caniggia Isabella
- Cantoni Lavinia
- Cao Lizhi
- Caplan Allan B.
- Caraglia Michele
- Cardinali Claudio
- Cardoso Sandra Morais
- Carew Jennifer S.
- Carleton Laura A.
- Carlin Cathleen R.
- Carloni Silvia
- Carlsson Sven R.
- Carmona-Gutierrez Didac
- Carneiro Leticia A. M.
- Carnevali Oliana
- Carra Serena
- Carrier Alice
- Carroll Bernadette
- Casas Caty
- Casas Josefina
- Cassinelli Giuliana
- Castets Perrine
- Castro-Obregon Susana
- Cavallini Gabriella
- Ceccherini Isabella
- Cecconi Francesco
- Cederbaum Arthur I.
- Cenci Simone
- Cerella Claudia
- Cervia Davide
- Cetrullo Silvia
- Ceña Valentín
- Chaachouay Hassan
- Chae Han-Jung
- Chagin Andrei S.
- Chai Chee-Yin
- Chakrabarti Gopal
- Chamilos Georgios
- Chan Edmond Y. W.
- Chan Matthew T. V.
- Chandra Dhyan
- Chandra Pallavi
- Chang Chih-Peng
- Chang Raymond Chuen-Chung
- Chang Ta Yuan
- Chatham John C.
- Chatterjee Saurabh
- Chauhan Santosh
- Che Yongsheng
- Cheetham Michael E.
- Cheluvappa Rajkumar
- Chen Chun-Jung
- Chen Gang
- Chen Guang-Chao
- Chen Guoqiang
- Chen Hongzhuan
- Chen Jeff W.
- Chen Jian-Kang
- Chen Min
- Chen Mingzhou
- Chen Peiwen
- Chen Qi
- Chen Quan
- Chen Shang-Der
- Chen Si
- Chen Steve S. -L.
- Chen Wei
- Chen Wei-Jung
- Chen Wen Qiang
- Chen Wenli
- Chen Xiangmei
- Chen Yau-Hung
- Chen Ye-Guang
- Chen Yin
- Chen Yingyu
- Chen Yongshun
- Chen Yu-Jen
- Chen Yue-Qin
- Chen Yujie
- Chen Zhen
- Chen Zhong
- Cheng Alan
- Cheng Christopher H. K.
- Cheng Hua
- Cheong Heesun
- Cherry Sara
- Chesney Jason
- Cheung Chun Hei Antonio
- Chevet Eric
- Chi Hsiang Cheng
- Chi Sung-Gil
- Chiacchiera Fulvio
- Chiang Hui-Ling
- Chiarelli Roberto
- Chiariello Mario
- Chieppa Marcello
- Chin Lih-Shen
- Chiong Mario
- Chiu Gigi N. C.
- Cho Dong-Hyung
- Cho Ssang-Goo
- Cho William C.
- Cho Yong-Yeon
- Cho Young-Seok
- Choi Augustine M. K.
- Choi Eui-Ju
- Choi Eun-Kyoung
- Choi Jayoung
- Choi Mary E.
- Choi Seung-Il
- Chou Tsui-Fen
- Chouaib Salem
- Choubey Divaker
- Choubey Vinay
- Chow Kuan-Chih
- Chowdhury Kamal
- Chu Charleen T.
- Chuang Tsung-Hsien
- Chun Taehoon
- Chung Hyewon
- Chung Taijoon
- Chung Yuen-Li
- Chwae Yong-Joon
- Cianfanelli Valentina
- Ciarcia Roberto
- Ciechomska Iwona A.
- Ciriolo Maria Rosa
- Cirone Mara
- Claerhout Sofie
- Clague Michael J.
- Clair Daret St
- Clarke Peter G. H.
- Clarke Robert
- Clementi Emilio
- Cleyrat Cédric
- Cl� ria Joan
- Cnop Miriam
- Coccia Eliana M.
- Cocco Tiziana
- Codogno Patrice
- Coers Jörn
- Cohen Ezra E. W.
- Colecchia David
- Coletto Luisa
- Coll Núria S.
- Colucci-Guyon Emma
- Comincini Sergio
- Condello Maria
- Cook Katherine L.
- Coombs Graham H.
- Cooper Cynthia D.
- Cooper J. Mark
- Coppens Isabelle
- Corasaniti Maria Tiziana
- Corazzari Marco
- Corbalan Ramon
- Corcelle-Termeau Elisabeth
- Cordero Mario D.
- Corral-Ramos Cristina
- Corti Olga
- Cossarizza Andrea
- Costelli Paola
- Costes Safia
- Cotman Susan L.
- Coto-Montes Ana
- Cottet Sandra
- Couve Eduardo
- Covey Lori R.
- Cowart L. Ashley
- Cox Jeffery S.
- Coxon Fraser P.
- Coyne Carolyn B.
- Cragg Mark S.
- Craven Rolf J.
- Crepaldi Tiziana
- Crespo Jose L.
- Criollo Alfredo
- Crippa Valeria
- Cruz Maria Teresa
- Cuervo Ana Maria
- Cuezva Jose M.
- Cui Taixing
- Cutillas Pedro R.
- Czaja Mark J.
- Czyzyk-Krzeska Maria F.
- D'amelio Marcello
- D'orazi Gabriella
- Dagda Ruben K.
- Dahmen Uta
- Dai Chunsun
- Dai Wenjie
- Dai Yun
- Dalby Kevin N.
- Dalmasso Guillaume
- Damme Markus
- Darfeuille-Michaud Arlette
- Dargemont Catherine
- Darley-Usmar Victor M.
- Dasarathy Srinivasan
- Dasgupta Biplab
- Dash Srikanta
- Dass Crispin R.
- Davey Hazel Marie
- Davids Lester M.
- Davis Roger J.
- Dawson Ted M.
- Dawson Valina L.
- Daza Paula
- de Belleroche Jackie
- de Cordoba Santiago Rodriguez
- de Figueiredo Paul
- de Figueiredo Regina Celia Bressan Queiroz
- de la Cruz Verónica Pérez
- de la Fuente José
- De Martino Luisa
- De Matteis Antonella
- de Melo Edesio Jose Tenorio
- De Meyer Guido R. Y.
- De Milito Angelo
- De Santi Mauro
- de Souza Wanderley
- De Tata Vincenzo
- De Zio Daniela
- Debnath Jayanta
- Dechant Reinhard
- Decuypere Jean-Paul
- Deegan Shane
- Dehay Benjamin
- Del Bello Barbara
- Del Re Dominic P.
- Delage-Mourroux Régis
- Delbridge Lea M. D.
- Deldicque Louise
- Delorme-Axford Elizabeth
- Deng Yizhen
- Dengjel Joern
- Denizot Melanie
- Dent Paul
- Der Channing J.
- Deretic Vojo
- Derrien Benoît
- Deutsch Eric
- Devarenne Timothy P.
- Devenish Rodney J.
- Di Antonio Aaron
- Di Bartolomeo Sabrina
- Di Daniele Nicola
- Di Domenico Fabio
- Di Nardo Alessia
- Di Paola Simone
- Di Pietro Antonio
- Di Renzo Livia
- Diaz-Meco Maria T.
- Diaz-Nido Javier
- Dickey Chad A.
- Dickson Robert C.
- Diederich Marc
- Digard Paul
- Dikic Ivan
- Dinesh-Kumar Savithrama P.
- Ding Chan
- Ding Wen-Xing
- Ding Zufeng
- Dini Luciana
- Distler Jörg H. W.
- Diwan Abhinav
- Djavaheri-Mergny Mojgan
- Dmytruk Kostyantyn
- Dobson Renwick C. J.
- Doetsch Volker
- Dokladny Karol
- Dokudovskaya Svetlana
- Donadelli Massimo
- Dong X. Charlie
- Dong Xiaonan
- Dong Zheng
- Donohue Terrence M.
- Donohue-Jr Terrence M.
- Doran Kelly S.
- Dorn Gerald W.
- Dos Santos Claudia Nunes
- Dosenko Victor
- Dridi Sami
- Drucker Liat
- du Toit André
- Du Jie
- Du Li-Lin
- Du Lihuan
- Dua Priyamvada
- Duan Lei
- Duann Pu
- Dubey Vikash Kumar
- Duchen Michael R.
- Duchosal Michel A.
- Duez Helene
- Dugail Isabelle
- Dumit Verónica I.
- Duncan Mara C.
- Dunlop Elaine A.
- Dunn William A.
- Dupont Nicolas
- Dupuis Luc
- Durcan Thomas M.
- Durán Raúl V.
- Duvezin-Caubet Stéphane
- Duvvuri Umamaheswar
- Dávila David
- Díaz-Araya Guillermo
- Díaz-Laviada Ines
- Eapen Vinay
- Ebrahimi-Fakhari Darius
- Echard Arnaud
- Eckhart Leopold
- Edelstein Charles L.
- Edinger Aimee L.
- Eichinger Ludwig
- Eisenberg Tobias
- Eisenberg-Lerner Avital
- Eissa N. Tony
- El-Deiry Wafik S.
- El-Khoury Victoria
- Elazar Zvulun
- Eldar-Finkelman Hagit
- Elliott Chris J. H.
- Emanuele Enzo
- Emmenegger Urban
- Engedal Nikolai
- Engelbrecht Anna-Mart
- Engelender Simone
- Enserink Jorrit M.
- Erdmann Ralf
- Erenpreisa Jekaterina
- Eri Rajaraman
- Eriksen Jason L.
- Erman Andreja
- Escalante Ricardo
- Eskelinen Eeva-Liisa
- Espert Lucile
- Esteban-Martínez Lorena
- Evans Thomas J.
- Fabri Mario
- Fabrias Gemma
- Fabrizi Cinzia
- Facchiano Antonio
- Faggioni Alberto
- Fairlie W. Douglas
- Fan Chunhai
- Fan Daping
- Fan Jie
- Fang Shengyun
- Fanto Manolis
- Fanzani Alessandro
- Farkas Thomas
- Faure Mathias
- Favier Francois B.
- Fearnhead Howard
- Federici Massimo
- Fei Erkang
- Felizardo Tania C.
- Feng Hua
- Feng Yibin
- Feng Yuchen
- Ferguson Thomas A.
- Fernandez-Barrena Maite G.
- Fernandez-Checa Jose C.
- Fernandez-Zapico Martin E.
- Fernández Álvaro F.
- Fernández-López Arsenio
- Feron Olivier
- Ferraro Elisabetta
- Ferreira-Halder Carmen Veríssima
- Fesus Laszlo
- Feuer Ralph
- Fiesel Fabienne C.
- Filippi-Chiela Eduardo C.
- Filomeni Giuseppe
- Fimia Gian Maria
- Fingert John H.
- Finkbeiner Steven
- Finkel Toren
- Fiorito Filomena
- Fisher Paul B.
- Flajolet Marc
- Flamigni Flavio
- Florey Oliver
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- Wang Mei
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- Wang Yipeng
- Wang Yu
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- Wang Zhi-Nong
- Wappner Pablo
- Ward Carl
- Ward Diane McVey
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- Weis Simone Nardin
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- Weyand Cornelia M.
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- Wildenberg Manon E.
- Wileman Tom
- Wilkinson Deepti Srinivas
- Wilkinson Simon
- Willbold Dieter
- Williams Chris
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- Winklhofer Konstanze F.
- Witkin Steven S.
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- Xilouri Maria
- Xiong Yuyan
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- Xu Feng
- Xu Haoxing
- Xu Hongwei
- Xu Jian
- Xu Jianzhen
- Xu Jinxian
- Xu Liang
- Xu Xiaolei
- Xu Yangqing
- Xu Ye
- Xu Zhi-Xiang
- Xu Ziheng
- Xue Yu
- Yamada Takahiro
- Yamamoto Ai
- Yamanaka Koji
- Yamashina Shunhei
- Yamashiro Shigeko
- Yan Bing
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- Yan Zhen
- Yanagi Yasuo
- Yang Dun-Sheng
- Yang Jin-Ming
- Yang Liu
- Yang Minghua
- Yang Pei-Ming
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- Yang Qian
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- Yang Ying
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- Yang Zhihong
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- Yao Pamela J.
- Yao Xiaofeng
- Yao Zhenyu
- Yao Zhiyuan
- Yasui Linda S.
- Ye Mingxiang
- Yedvobnick Barry
- Yeganeh Behzad
- Yeh Elizabeth S.
- Yeyati Patricia L.
- Yi Fan
- Yi Long
- Yin Xiao-Ming
- Yip Calvin K.
- Yoo Yeong-Min
- Yoo Young Hyun
- Yoon Seung-Yong
- Yoshida Ken-Ichi
- Yoshimori Tamotsu
- Young Ken H.
- Yu Huixin
- Yu Jane J.
- Yu Jin-Tai
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- Yu W. Haung
- Yu Xiao-Fang
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- Yuan Junying
- Yuan Zhi-Min
- Yue Beatrice Y. J. T.
- Yue Jianbo
- Yue Zhenyu
- Zacks David N.
- Zacksenhaus Eldad
- Zaffaroni Nadia
- Zaglia Tania
- Zakeri Zahra
- Zecchini Vincent
- Zeng Jinsheng
- Zeng Min
- Zeng Qi
- Zervos Antonis S.
- Zhang Donna D.
- Zhang Fan
- Zhang Guo
- Zhang Guo-Chang
- Zhang Hao
- Zhang Hong
- Zhang Hongbing
- Zhang Jian
- Zhang Jiangwei
- Zhang Jianhua
- Zhang Jing-Pu
- Zhang Li
- Zhang Lin
- Zhang Long
- Zhang Ming-Yong
- Zhang Xiangnan
- Zhang Xu Dong
- Zhang Yan
- Zhang Yang
- Zhang Yanjin
- Zhang Yingmei
- Zhang Yunjiao
- Zhao Mei
- Zhao Wei-Li
- Zhao Xiaonan
- Zhao Yan G.
- Zhao Ying
- Zhao Yongchao
- Zhao Yu-Xia
- Zhao Zhendong
- Zhao Zhizhuang J.
- Zheng Dexian
- Zheng Xi-Long
- Zheng Xiaoxiang
- Zhivotovsky Boris
- Zhong Qing
- Zhou Guang-Zhou
- Zhou Guofei
- Zhou Huiping
- Zhou Shu-Feng
- Zhou Xu-Jie
- Zhu Hongxin
- Zhu Hua
- Zhu Wei-Guo
- Zhu Wenhua
- Zhu Xiao-Feng
- Zhu Yuhua
- Zhuang Shi-Mei
- Zhuang Xiaohong
- Ziparo Elio
- Zois Christos E.
- Zoladek Teresa
- Zong Wei-Xing
- Zorzano Antonio
- Zughaier Susu M.
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2016
- Field of study
non present
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
- Author
- Abdelmohsen Kotb
- Abe Akihisa
- Abedin Md Joynal
- Abeliovich Hagai
- Adachi Hiroaki
- Adams Christopher M.
- Adams Peter D.
- Adeli Khosrow
- Adhihetty Peter J.
- Adler Sharon G.
- Agam Galila
- Agarwal Rajesh
- Aghi Manish K.
- Agnello Maria
- Agostinis Patrizia
- Aguilar Patricia V.
- Aguirre-Ghiso Julio
- Airoldi Edoardo M.
- Ait-Si-Ali Slimane
- Akematsu Takahiko
- Akporiaye Emmanuel T.
- Al-Rubeai Mohamed
- Albaiceta Guillermo M.
- Albanese Chris
- Albani Diego
- Albert Matthew L.
- Aldudo Jesus
- Alguel Hana
- Alirezaei Mehrdad
- Alloza Iraide
- Almasan Alexandru
- Almonte-Beceril Maylin
- Alnemri Emad S.
- Alonso Covadonga
- Altan-Bonnet Nihal
- Altieri Dario C.
- Alvarez Silvia
- Alvarez-Erviti Lydia
- Alves Sandro
- Amadoro Giuseppina
- Amano Atsuo
- Amantini Consuelo
- Ambrosio Santiago
- Amelio Ivano
- Amer Amal O.
- Amessou Mohamed
- Amon Angelika
- An Zhenyi
- Ana Gonzalez-Polo Rosa
- Anania Frank A.
- Andersen Stig U.
- Andley Usha P.
- Andreadi Catherine K.
- Andrieu-Abadie Nathalie
- Anel Alberto
- Ann David K.
- Anoopkumar-Dukie Shailendra
- Antonioli Manuela
- Aoki Hiroshi
- Apostolova Nadezda
- Aquila Saveria
- Aquilano Katia
- Araki Koichi
- Arama Eli
- Aranda Agustin
- Araya Jun
- Arcaro Alexandre
- Arias Esperanza
- Arimoto Hirokazu
- Ariosa Aileen R.
- Armstrong Jane L.
- Arnould Thierry
- Arozena Abraham Acevedo
- Arsov Ivica
- Asanuma Katsuhiko
- Askanas Valerie
- Asselin Eric
- Atarashi Ryuichiro
- Atherton Sally S.
- Atkin Julie D.
- Attardi Laura D.
- Auberger Patrick
- Auburger Georg
- Aurelian Laure
- Autelli Riccardo
- Avagliano Laura
- Avantaggiati Maria Laura
- Avrahami Limor
- Awale Suresh
- Azad Neelam
- Bachetti Tiziana
- Backer Jonathan M.
- Bae Dong-Hun
- Bae Jae-Sung
- Bae Ok-Nam
- Bae Soo Han
- Baehrecke Eric H.
- Baek Seung-Hoon
- Baghdiguian Stephen
- Bagniewska-Zadworna Agnieszka
- Bai Hua
- Bai Jie
- Bai Xue-Yuan
- Bailly Yannick
- Balaji Kithiganahalli Narayanaswamy
- Balduini Walter
- Ballabio Andrea
- Balzan Rena
- Banerjee Rajkumar
- Banhegyi Gabor
- Bao Haijun
- Barbato Daniele Lettieri
- Barbeau Benoit
- Barrachina Maria D.
- Barreiro Esther
- Bartel Bonnie
- Bartolome Alberto
- Bassham Diane C.
- Bassi Maria Teresa
- Bast Robert C., Jr.
- Basu Alakananda
- Batista Maria Teresa
- Batoko Henri
- Battino Maurizio
- Bauckman Kyle
- Baumgarner Bradley L.
- Bayer K. Ulrich
- Beale Rupert
- Beaulieu Jean-Francois
- Beck George R., Jr.
- Becker Christoph
- Beckham J. David
- Bedard Pierre-Andre
- Bednarski Patrick J.
- Begley Thomas J.
- Behl Christian
- Behrends Christian
- Behrens Georg M. N.
- Behrns Kevin E.
- Bejarano Eloy
- Belaid Amine
- Belleudi Francesca
- Benard Giovanni
- Berchem Guy
- Bergamaschi Daniele
- Bergami Matteo
- Berkhout Ben
- Berliocchi Laura
- Bernard Amelie
- Bernard Monique
- Bernassola Francesca
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- Udelnow Andrej
- Ueno Takashi
- Umekawa Midori
- Umemiya-Shirafuji Rika
- Underwood Benjamin R.
- Ungermann Christian
- Ureshino Rodrigo P.
- Ushioda Ryo
- Uversky Vladimir N.
- Uzcategui Nestor L.
- Vaccari Thomas
- Vaccaro Maria I.
- Vachova Libuse
- Vakifahmetoglu-Norberg Helin
- Valdor Rut
- Valente Enza Maria
- Valle Luisa Dalla
- Vallette Francois
- Valverde Angela M.
- van Campagne Menno Lookeren
- Van den Berghe Greet
- Van Den Bosch Ludo
- van den Brink Gijs R.
- van der Goot F. Gisou
- van der Klei Ida J.
- van der Laan Luc J. W.
- van Doorn Wouter G.
- van Egmond Marjolein
- van Golen Kenneth L.
- Van Kaer Luc
- Vandenabeele Peter
- Vandenberghe Wim
- Vanhorebeek Ilse
- Varela-Nieto Isabel
- Vasconcelos M. Helena
- Vasko Radovan
- Vavvas Demetrios G.
- Vega-Naredo Ignacio
- Velasco Guillermo
- Velentzas Athanassios D.
- Velentzas Panagiotis D.
- Vellai Tibor
- Vellenga Edo
- Vendelbo Mikkel Holm
- Venkatachalam Kartik
- Ventura Natascia
- Ventura Salvador
- Veras Patricia S. T.
- Verdier Mireille
- Vertessy Beata G.
- Vescovi Eleonora Garcia
- Viale Andrea
- Vidal Michel
- Vieira Helena L. A.
- Vierstra Richard D.
- Vigneswaran Nadarajah
- Vij Neeraj
- Vila Miquel
- Villar Margarita
- Villar Victor H.
- Villarroya Joan
- Vindis Cecile
- Viola Giampietro
- Viscomi Maria Teresa
- Vitale Giovanni
- Vogl Dan T.
- Voitsekhovskaja Olga V.
- von Haefen Clarissa
- von Schwarzenberg Karin
- Voth Daniel E.
- Vouret-Craviari Valerie
- Vuori Kristina
- Vyas Jatin M.
- Waeber Christian
- Walker Cheryl Lyn
- Walker Mark J.
- Walter Jochen
- Wan Lei
- Wan Xiangbo
- Wang Bo
- Wang Caihong
- Wang Chao-Yung
- Wang Chengshu
- Wang Chenran
- Wang Chuangui
- Wang Dong
- Wang Fen
- Wang Fuxin
- Wang Guanghui
- Wang Hai-jie
- Wang Haichao
- Wang Hong-Gang
- Wang Hongmin
- Wang Horng-Dar
- Wang Jing
- Wang Junjun
- Wang Mei
- Wang Mei-Qing
- Wang Pei-Yu
- Wang Peng
- Wang Richard C.
- Wang Shuo
- Wang Ting-Fang
- Wang Xian
- Wang Xiao-jia
- Wang Xiao-Wei
- Wang Xin
- Wang Xuejun
- Wang Yan
- Wang Yanming
- Wang Ying
- Wang Ying-Jan
- Wang Yipeng
- Wang Yu
- Wang Yu Tian
- Wang Yuqing
- Wang Zhi-Nong
- Wappner Pablo
- Ward Carl
- Ward Diane Mcvey
- Warnes Gary
- Watada Hirotaka
- Watanabe Yoshihisa
- Watase Kei
- Weaver Timothy E.
- Weekes Colin D.
- Wei Jiwu
- Weide Thomas
- Weihl Conrad C.
- Weindl Guenther
- Weis Simone Nardin
- Wen Longping
- Wen Xin
- Wen Yunfei
- Westermann Benedikt
- Weyand Cornelia M.
- White Anthony R.
- White Eileen
- Whitton J. Lindsay
- Whitworth Alexander J.
- Wiels Joelle
- Wild Franziska
- Wildenberg Manon E.
- Wileman Tom
- Wilkinson Deepti Srinivas
- Wilkinson Simon
- Willbold Dieter
- Williams Chris
- Williams Katherine
- Williamson Peter R.
- Winklhofer Konstanze F.
- Witkin Steven S.
- Wohlgemuth Stephanie E.
- Wollert Thomas
- Wolvetang Ernst J.
- Wong Esther
- Wong G. William
- Wong Richard W.
- Wong Vincent Kam Wai
- Woodcock Elizabeth A.
- Wright Karen L.
- Wu Chunlai
- Wu Defeng
- Wu Gen Sheng
- Wu Jian
- Wu Junfang
- Wu Mian
- Wu Min
- Wu Shengzhou
- Wu William K. K.
- Wu Yaohua
- Wu Zhenlong
- Xavier Cristina P. R.
- Xavier Ramnik J.
- Xia Gui-Xian
- Xia Tian
- Xia Weiliang
- Xia Yong
- Xiao Hengyi
- Xiao Jian
- Xiao Shi
- Xiao Wuhan
- Xie Chuan-Ming
- Xie Zhiping
- Xie Zhonglin
- Xilouri Maria
- Xiong Yuyan
- Xu Chuanshan
- Xu Congfeng
- Xu Feng
- Xu Haoxing
- Xu Hongwei
- Xu Jian
- Xu Jianzhen
- Xu Jinxian
- Xu Liang
- Xu Xiaolei
- Xu Yangqing
- Xu Ye
- Xu Zhi-Xiang
- Xu Ziheng
- Xue Yu
- Yamada Takahiro
- Yamamoto Ai
- Yamanaka Koji
- Yamashina Shunhei
- Yamashiro Shigeko
- Yan Bing
- Yan Bo
- Yan Xianghua
- Yan Zhen
- Yanagi Yasuo
- Yang Dun-Sheng
- Yang Jin-Ming
- Yang Liu
- Yang Minghua
- Yang Pei-Ming
- Yang Peixin
- Yang Qian
- Yang Wannian
- Yang Wei Yuan
- Yang Xuesong
- Yang Yi
- Yang Ying
- Yang Zhifen
- Yang Zhihong
- Yao Meng-Chao
- Yao Pamela J.
- Yao Xiaofeng
- Yao Zhenyu
- Yao Zhiyuan
- Yasui Linda S.
- Ye Mingxiang
- Yedvobnick Barry
- Yeganeh Behzad
- Yeh Elizabeth S.
- Yeyati Patricia L.
- Yi Fan
- Yi Long
- Yin Xiao-Ming
- Yip Calvin K.
- Yoo Yeong-Min
- Yoo Young Hyun
- Yoon Seung-Yong
- Yoshida Ken-Ichi
- Yoshimori Tamotsu
- Young Ken H.
- Yu Huixin
- Yu Jane J.
- Yu Jin-Tai
- Yu Jun
- Yu Li
- Yu W. Haung
- Yu Xiao-Fang
- Yu Zhengping
- Yuan Junying
- Yuan Zhi-Min
- Yue Beatrice Y. J. T.
- Yue Jianbo
- Yue Zhenyu
- Zacks David N.
- Zacksenhaus Eldad
- Zaffaroni Nadia
- Zaglia Tania
- Zakeri Zahra
- Zecchini Vincent
- Zeng Jinsheng
- Zeng Min
- Zeng Qi
- Zervos Antonis S.
- Zhang Donna D.
- Zhang Fan
- Zhang Guo
- Zhang Guo-Chang
- Zhang Hao
- Zhang Hong
- Zhang Hong
- Zhang Hongbing
- Zhang Jian
- Zhang Jian
- Zhang Jiangwei
- Zhang Jianhua
- Zhang Jing-pu
- Zhang Li
- Zhang Lin
- Zhang Lin
- Zhang Long
- Zhang Ming-Yong
- Zhang Xiangnan
- Zhang Xu Dong
- Zhang Yan
- Zhang Yang
- Zhang Yanjin
- Zhang Yingmei
- Zhang Yunjiao
- Zhao Mei
- Zhao Wei-Li
- Zhao Xiaonan
- Zhao Yan G.
- Zhao Ying
- Zhao Yongchao
- Zhao Yu-Xia
- Zhao Zhendong
- Zhao Zhizhuang J.
- Zheng Dexian
- Zheng Xi-Long
- Zheng Xiaoxiang
- Zhivotovsky Boris
- Zhong Qing
- Zhou Guang-Zhou
- Zhou Guofei
- Zhou Huiping
- Zhou Shu-Feng
- Zhou Xu-Jie
- Zhu Hongxin
- Zhu Hua
- Zhu Wei-Guo
- Zhu Wenhua
- Zhu Xiao-Feng
- Zhu Yuhua
- Zhuang Shi-Mei
- Zhuang Xiaohong
- Ziparo Elio
- Zois Christos E.
- Zoladek Teresa
- Zong Wei-Xing
- Zorzano Antonio
- Zughaier Susu M.
- Publication venue
- Publication date
- 01/01/2016
- Field of study