46 research outputs found
A C19MC-LIN28A-MYCN Oncogenic Circuit Driven by Hijacked Super-enhancers Is a Distinct Therapeutic Vulnerability in ETMRs: A Lethal Brain Tumor
- Author
- Barsyte-Lovejoy Dalia
- Bouffet Eric
- Catchpoole Daniel
- Chan Jennifer
- Dirks Peter B.
- Du Yuchen
- Ellezam Benjamin
- Fan Xiaolian
- Fangusaro Jason
- Fouladi Maryam
- Gillespie G. Yancey
- Grundy Richard G.
- Guilhamon Paul
- Gupta Nalin
- Hansford Jordan R.
- Hawkins Cynthia E.
- Ho Ben
- Hoffman Lindsey M.
- Huang Annie
- Hwang Eugene I.
- Jabado Nada
- Johnston Donna
- Kim Seung-Ki
- Kleinman Claudia L.
- Lafay-Cousin Lucie
- Lassaletta Alvaro
- Leary Sarah
- Li Xiao-Nan
- Lin Charles Y.
- Lindsay Holly
- Lu Mei
- Mack Stephen C.
- Massimi Luca
- Michaud Jean
- Mulcahy Levy Jean M.
- Mumal Iqra
- Nakamura Hideo
- Patel Neilket
- Popovski Dean
- Ra Young-Shin
- Ramanujachar Ramya
- Reddy Alyssa
- Rich Jeremy N.
- Rivas Eloy
- Sin-Chan Patrick
- Singh Irtisha
- Singh Sheila K.
- Solano-Paez Palma
- Suwal Tannu
- Taylor Michael D.
- Torchia Jonathon
- Van Meter Timothy E.
- Wang Yin
- Wong Tai-Tong
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2019
- Field of study
© 2019 Elsevier Inc. Embryonal tumors with multilayered rosettes (ETMRs) are highly lethal infant brain cancers with characteristic amplification of Chr19q13.41 miRNA cluster (C19MC) and enrichment of pluripotency factor LIN28A. Here we investigated C19MC oncogenic mechanisms and discovered a C19MC-LIN28A-MYCN circuit fueled by multiple complex regulatory loops including an MYCN core transcriptional network and super-enhancers resulting from long-range MYCN DNA interactions and C19MC gene fusions. Our data show that this powerful oncogenic circuit, which entraps an early neural lineage network, is potently abrogated by bromodomain inhibitor JQ1, leading to ETMR cell death. Sin-Chan et al. uncover a C19MC-LIN28A-MYCN super-enhancer-dependent oncogenic circuit in embryonal tumors with multilayered rosettes (ETMRs). The circuit entraps an early neural lineage network to sustain embryonic epigenetic programming and is vulnerable to bromodomain inhibition, which promotes ETMR cell death
Therapeutic and Prognostic Implications of BRAF V600E in Pediatric Low-Grade Gliomas.
- Author
- Arnoldo Anthony
- Bartels Ute
- Bouffet Eric
- Carret Anne Sophie
- Chan Aden
- Chen Shiyi
- Crane Courtney
- Cruz Ofelia
- Dalton James D
- de Torres Carmen
- Dirks Peter
- Eisenstat David
- Ellison David W
- Faure Conter Cécile
- Finch Elizabeth
- Fleming Adam
- Foreman Nicholas
- Frappaz Didier
- Garre Maria Luisa
- Giannini Caterina
- Guerreiro Stucklin Ana
- Harreld Julie H
- Hauser Peter
- Hawkins Cynthia
- Ho Cheng-Ying
- Honnorat Marion
- Huang Annie
- Jabado Nada
- Karajannis Matthias A
- Kieran Mark
- Krishnatry Rahul
- Krskova Lenka
- Larouche Valerie
- Lassaletta Alvaro
- Leary Sarah
- Ligon Keith L
- Ling Catriona
- Loukides Jim
- Mao Ying
- Mascelli Samantha
- McKeown Tara
- Mistry Matthew
- Mueller Sabine
- Mulcahy-Levy Jean
- Nageswara Rao Amulya
- Ng Ho-Keung
- Nicolaides Theodore
- Nozza Paolo
- Packer Roger J
- Perbet Romain
- Qaddoumi Ibrahim
- Ramaswamy Vijay
- Raso Alessandro
- Rutka James T
- Ryall Scott
- Shi Zhi-Feng
- Silva Karen
- Snuderl Matija
- Sumerauer David
- Tabori Uri
- Tatevossian Ruth
- Taylor Michael D
- Vasiljevic Alexandre
- Wang Shiyang
- Wilson Bev
- Zapotocky Michal
- Zelcer Shayna
- Zhukova Nataliya
- Publication venue
- Scholarship@Western
- Publication date
- 01/01/2017
- Field of study
Purpose BRAF V600E is a potentially highly targetable mutation detected in a subset of pediatric low-grade gliomas (PLGGs). Its biologic and clinical effect within this diverse group of tumors remains unknown.
Patients and Methods A combined clinical and genetic institutional study of patients with PLGGs with long-term follow-up was performed (N = 510). Clinical and treatment data of patients with BRAF V600E mutated PLGG (n = 99) were compared with a large international independent cohort of patients with BRAF V600E mutated-PLGG (n = 180).
Results BRAF V600E mutation was detected in 69 of 405 patients (17%) with PLGG across a broad spectrum of histologies and sites, including midline locations, which are not often routinely biopsied in clinical practice. Patients with BRAF V600E PLGG exhibited poor outcomes after chemotherapy and radiation therapies that resulted in a 10-year progression-free survival of 27% (95% CI, 12.1% to 41.9%) and 60.2% (95% CI, 53.3% to 67.1%) for BRAF V600E and wild-type PLGG, respectively ( P \u3c .001). Additional multivariable clinical and molecular stratification revealed that the extent of resection and CDKN2A deletion contributed independently to poor outcome in BRAF V600E PLGG. A similar independent role for CDKN2A and resection on outcome were observed in the independent cohort. Quantitative imaging analysis revealed progressive disease and a lack of response to conventional chemotherapy in most patients with BRAF V600E PLGG.
Conclusion BRAF V600E PLGG constitutes a distinct entity with poor prognosis when treated with current adjuvant therapy
Therapeutic and Prognostic Implications of BRAF V600E in Pediatric Low-Grade Gliomas
- Author
- Adam Fleming
- Aden Chan
- Alessandro Raso
- Alexandre Vasiljevic
- Alvaro Lassaletta
- Amulya Nageswara Rao
- Ana Guerreiro Stucklin
- Anne Sophie Carret
- Annie Huang
- Anthony Arnoldo
- Bergthold G
- Bev Wilson
- Carmen de Torres
- Caterina Giannini
- Catriona Ling
- Cheng-Ying Ho
- Courtney Crane
- Cynthia Hawkins
- Cécile Faure Conter
- David Eisenstat
- David Sumerauer
- David W. Ellison
- Didier Frappaz
- Elizabeth Finch
- Eric Bouffet
- Ho-Keung Ng
- Ibrahim Qaddoumi
- James D. Dalton
- James T. Rutka
- Jean Mulcahy-Levy
- Jim Loukides
- Julie H. Harreld
- Karen Silva
- Keith L. Ligon
- Lenka Krskova
- Maria Luisa Garre
- Marion Honnorat
- Mark Kieran
- Matija Snuderl
- Matthew Mistry
- Matthias A. Karajannis
- Michael D. Taylor
- Michal Zapotocky
- Nada Jabado
- Nataliya Zhukova
- Nicholas Foreman
- Ofelia Cruz
- Paolo Nozza
- Peter Dirks
- Peter Hauser
- Rahul Krishnatry
- Roger J. Packer
- Romain Perbet
- Ruth Tatevossian
- Sabine Mueller
- Samantha Mascelli
- Sarah Leary
- Scott Ryall
- Shayna Zelcer
- Shiyang Wang
- Shiyi Chen
- Tara McKeown
- Theodore Nicolaides
- Uri Tabori
- Ute Bartels
- Valerie Larouche
- Vijay Ramaswamy
- Ying Mao
- Zhi-Feng Shi
- Publication venue
- 'American Society of Clinical Oncology (ASCO)'
- Publication date
- 01/01/2017
- Field of study
Purpose BRAF V600E is a potentially highly targetable mutation detected in a subset of pediatric low-grade gliomas (PLGGs). Its biologic and clinical effect within this diverse group of tumors remains unknown. Patients and Methods A combined clinical and genetic institutional study of patients with PLGGs with long-term follow-up was performed (N = 510). Clinical and treatment data of patients with BRAF V600E mutated PLGG (n = 99) were compared with a large international independent cohort of patients with BRAF V600E mutated-PLGG (n = 180). Results BRAF V600E mutation was detected in 69 of 405 patients (17%) with PLGG across a broad spectrum of histologies and sites, including midline locations, which are not often routinely biopsied in clinical practice. Patients with BRAF V600E PLGG exhibited poor outcomes after chemotherapy and radiation therapies that resulted in a 10-year progression-free survival of 27% (95% CI, 12.1% to 41.9%) and 60.2% (95% CI, 53.3% to 67.1%) for BRAF V600E and wild-type PLGG, respectively (P < .001). Additional multivariable clinical and molecular stratification revealed that the extent of resection and CDKN2A deletion contributed independently to poor outcome in BRAF V600E PLGG. A similar independent role for CDKN2A and resection on outcome were observed in the independent cohort. Quantitative imaging analysis revealed progressive disease and a lack of response to conventional chemotherapy in most patients with BRAF V600E PLGG. Conclusion BRAF V600E PLGG constitutes a distinct entity with poor prognosis when treated with current adjuvant therapy. (C) 2017 by American Society of Clinical Oncolog
Reduced costs with bisoprolol treatment for heart failure - An economic analysis of the second Cardiac Insufficiency Bisoprolol Study (CIBIS-II)
- Author
- Achremczyk P
- Adgey J
- Ambepitiya G
- Anghern W
- Arab T
- Aronov DM
- Artaza M
- Arutjunov GP
- Aschermann M
- Assmann I
- Aumont MC
- Aupetit JF
- Bacquet P
- Baille N
- Bart BJ
- Basechikin SS
- Baudouy P
- Belenkov JN
- Belin A
- Beloussov JB
- Beyer T
- Bischoff KO
- Bokeria OA
- Boland J
- Bonneau A
- Bonneric G
- Boon N
- Bousser JP
- Boyle RM
- Bridges A
- Brunhuber W
- Bruthansl J
- Burgnard F
- Campos JMM
- Ceia MF
- Charchogljan RA
- Chaudron JM
- Ciampricotti R
- Citron B
- Conthe P
- Cowley AJ
- Crean P
- Cripps T
- Cruz JM
- Csanady M
- Cserhalmi L
- Cussac N
- Czestockowska E
- d'Ivernois C
- Dahlstrom U
- Dargie HJ
- Darius H
- Dary P
- Davies MK
- De Baker G
- De Groote P
- de Moura ALZC
- De Vito F
- Decoulx E
- DenHartog FR
- Denolle T
- Dievart F
- Doschytsin V
- Dowgird M
- Dubach P
- Dunn F
- Duriez P
- Dussous V
- Dyduszynski A
- Edes I
- Eicher JC
- Ekdahl S
- Enjuto G
- Erdmann E
- Erne P
- Ertl G
- Fedorova TA
- Ferriere M
- Findlay J
- Fleck E
- Fogari R
- Follath F
- Follath F
- Forsey P
- Forster K
- Fournier E
- Freytag F
- Funck-Brentano C
- Funck-Brentano C
- Fyfe T
- Galie N
- Gallino A
- Garandeau M
- Garcia-Moll M
- Gauthier J
- Genest M
- Gerbe A
- Gesztesi T
- Giani P
- Gleichmann U
- Glezer MG
- Godenir JP
- Goetzsche CO
- Gomes RS
- Gorbachenkov A
- Gorshkov
- Gorski J
- Gospodarenko AL
- Gould B
- Greenwood TW
- Groundstroem K
- Guillot B
- Guillot JP
- Guillot P
- Haasis R
- Haghfelt T
- Haise S
- Hansen JF
- Hansen S
- Henneman JA
- Heno P
- Henssge R
- Hesse P
- Hey D
- Hildebrandt P
- Hill C
- Hjelmaeus L
- Hofmann R
- Hofs T
- Hoglund C
- Hoglund C
- Hohnloser S
- Hombach V
- Hradec M
- Hubner P
- Ilmurzynska K
- Ivashkin VT
- Ivleva AJ
- Jaillon P
- Janicki K
- Jean M
- Jmouro AV
- Jordaens L
- Kacet S
- Kaliska G
- Kalle R
- Karpati P
- Kassis E
- Keck M
- Khan S
- Klein H
- Klein W
- Kolbel F
- Komajda M
- Korewicki J
- Kornacewicz-Jach Z
- Kragten JA
- Kraska T
- Kromer ET
- Kruls-Munch J
- Krzeminska-Pakula M
- Kuch J
- Kuhn P
- Kyrichenko AA
- Lacroix A
- Lallemand R
- Lardoux H
- Lavrov AA
- Lazebnik LB
- Le Heuzey JY
- Lechat P
- Leizorovicz A
- Levy E
- Lewis P
- Liem KL
- Limburg A
- Lindberg K
- Linssen GCM
- Lofdahl P
- Lopez-Sendon JL
- Lousada N
- Luderitz B
- Mackay A
- Maisch B
- Maltz M
- Marejev VJ
- Mareyev V
- Marquet M
- Martin M
- Martin O
- Martinez A
- Marynov A
- Mazaev VP
- McArthur J
- McCann H
- McGuire A
- McLeod A
- McLeod D
- McMurray J
- Melchior JP
- Merot JL
- Mery D
- Metcalfe M
- Milanese U
- Millar-Craig M
- Mills P
- Mitrovic V
- Moccetti T
- Monzon F
- Mossaz R
- Mothes P
- Mulcahy D
- Murin J
- Nartowicz E
- Nelson JK
- Nesser HJ
- Neubauer S
- Nicholls D
- Oakley GD
- Olive T
- Osterziel KJ
- Ostorero M
- Paganelli F
- Page E
- Paschen B
- Pasteuning H
- Patterson DLH
- Pauly-Laubry C
- Penn HJAM
- Petelenz T
- Piwowarska W
- Pohl JEF
- Polejev NR
- Preda I
- Providencia LA
- Puel J
- Rasmussen V
- Rawczynska-Englert I
- Ray S
- Remme WJ
- Remme WJ
- Ribas M
- Roig E
- Rokkedal J
- Roldan I
- Rolland C
- Rousseau JF
- Roux JJ
- Ruzyllo W
- Rybar R
- Sadowski Z
- Scalvini S
- Schaafsma HJ
- Schelling A
- Schenowitz A
- Scrutinio D
- Seabra-Gomes RJ
- Sechi L
- Semrad B
- Sendon JLL
- Shpektor
- Sidorenko BA
- Silke B
- Simon H
- Simon K
- Slany J
- Sloos R
- Sobolev KE
- Sourdais K
- Spitzer SG
- Starodoubtsev AK
- Stohring R
- Storozhakhov GI
- Sugrue D
- Swiatecka G
- Syrkin AL
- Szucs TD
- Tarjan J
- Taubert G
- Teichmann W
- Tendera M
- Tettamanti F
- Theisen K
- Thomassen A
- Tramarin R
- Tremel F
- Ulvenstam G
- Uusimaa P
- Valle V
- van Dantzig JM
- van der Burgh PH
- van der Linde MR
- van Hoogenhuyze DCA
- van Kesteren HAM
- van Mieghem W
- Van Rossum P
- Vanoli E
- Verdun A
- Verkenne P
- Warselius L
- Wehrlen-Grandjean M
- Weihs W
- Wende W
- Wesdorp JCL
- Wiedermann C
- Wiemann H
- Wierzchowiecki M
- Wieser H
- Wilkinson PR
- Wimmer H
- Witchiz S
- Wodniecki J
- Wojciechowoski D
- Wolf JE
- Wrabec K
- Wysocki H
- Zannad F
- Zodionchenko VS
- Zotz R
- Zvereva TV
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2001
- Field of study
Background
Beta-blockers, used as an adjunctive to diuretics, digoxin and angiotensin converting enzyme inhibitors, improve survival in chronic heart failure. We report a prospectively planned economic analysis of the cost of adjunctive beta-blocker therapy in the second Cardiac Insufficiency BIsoprolol Study (CIBIS II).
Methods
Resource utilization data (drug therapy, number of hospital admissions, length of hospital stay, ward type) were collected prospectively in all patients in CIBIS . These data were used to determine the additional direct costs incurred, and savings made, with bisoprolol therapy. As well as the cost of the drug, additional costs related to bisoprolol therapy were added to cover the supervision of treatment initiation and titration (four outpatient clinic/office visits). Per them (hospital bed day) costings were carried out for France, Germany and the U.K. Diagnosis related group costings were performed for France and the U.K. Our analyses took the perspective of a third party payer in France and Germany and the National Health Service in the U.K.
Results
Overall, fewer patients were hospitalized in the bisoprolol group, there were fewer hospital admissions perpatient hospitalized, fewer hospital admissions overall, fewer days spent in hospital and fewer days spent in the most expensive type of ward. As a consequence the cost of care in the bisoprolol group was 5-10% less in all three countries, in the per them analysis, even taking into account the cost of bisoprolol and the extra initiation/up-titration visits. The cost per patient treated in the placebo and bisoprolol groups was FF35 009 vs FF31 762 in France, DM11 563 vs DM10 784 in Germany and pound 4987 vs pound 4722 in the U.K. The diagnosis related group analysis gave similar results.
Interpretation
Not only did bisoprolol increase survival and reduce hospital admissions in CIBIS II, it also cut the cost of care in so doing. This `win-win' situation of positive health benefits associated with cost savings is Favourable from the point of view of both the patient and health care systems. These findings add further support for the use of beta-blockers in chronic heart failure
Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018.
- Author
- A Aouacheria
- A Aouacheria
- A Aranovich
- A Ashkenazi
- A Ashkenazi
- A Ashkenazi
- A Bernet
- A Buque
- A Chiche
- A Conte
- A Costanzo
- A Crockford
- A Degterev
- A Degterev
- A Dey
- A Gast
- A Gross
- A Hakkim
- A Hamacher-Brady
- A Hunger
- A Kaczmarek
- A Kamb
- A Koenig
- A Kotschy
- A Letai
- A Linkermann
- A Linkermann
- A Linkermann
- A Linkermann
- A Mousa
- A Muir
- A Mukherjee
- A Nilsson
- A Oberst
- A Oberst
- A Pagotto
- A Pyakurel
- A Rongvaux
- A Rubartelli
- A Sahaboglu
- A Seiler
- A Serrano-Puebla
- A Shamas-Din
- A Sistigu
- A Strasser
- A Strasser
- A Strasser
- A Strasser
- A Strasser
- A Strasser
- A Sumoza-Toledo
- A Sundararaman
- A Tittarelli
- A Trautmann
- A Villunger
- A Witt
- A Zychlinsky
- AA Fatokun
- AA Mailleux
- Aaron Ciechanover
- AB Pardee
- Abhishek D. Garg
- AC Bellail
- AC Schinzel
- AD Garg
- AD Garg
- AD Garg
- AD Garg
- AD Garg
- AD Garg
- AD Garg
- Adi Kimchi
- AE Alsop
- AE Feldstein
- AJ Schile
- AL Anding
- AL Genevois
- Alexey V. Antonov
- AM Chinnaiyan
- AM Distefano
- AM Dudek
- AM Verhagen
- AN Antony
- AN Barclay
- Ana J. García-Sáez
- Andreas Linkermann
- Andreas Strasser
- Andreas Villunger
- Andrew Oberst
- Andrew Thorburn
- Antonella Sistigu
- AP West
- AR Delbridge
- AT Schneider
- AT Ting
- AT Ting
- Atan Gross
- AV Follis
- AV Jacobsen
- AV Vaseva
- AV Vaseva
- AW Roberts
- B Antonsson
- B Aslan
- B Conradt
- B Fadeel
- B Gerlach
- B Gibert
- B Gooptu
- B McDonald
- B Schellenberg
- B Van Do
- B Xia
- BA Carlson
- BA Hilton
- BA Napier
- BB Aggarwal
- BC Barnhart
- Bertrand Joseph
- Beth Levine
- BG Childs
- BG Childs
- BG Childs
- BG Lambrus
- BG Yipp
- Boris Turk
- Boris Zhivotovsky
- BP Eckelman
- BP Eckelman
- BR Stockwell
- Brent R. Stockwell
- Brian D. Dynlacht
- BT Cookson
- C Bergmann
- C Dominguez-Brauer
- C Du
- C Frezza
- C Gerle
- C Guenebeaud
- C Gunther
- C Gunther
- C Helmke
- C Hernandez
- C Hockings
- C Lood
- C Lopez-Garcia
- C Lopez-Otin
- C Lopez-Otin
- C Louandre
- C Louandre
- C Nelson
- C Oberle
- C Piot
- C Rogers
- C Scaffidi
- C Vanpouille-Box
- C White
- C Xie
- Carlos López-Otín
- Carmen Garrido
- Catherine Brenner
- CC Wu
- CD Simpson
- CD Wiley
- Cecilia M.P. Rodrigues
- CF Wenceslau
- Christoph Borner
- CJ Kearney
- CK Ea
- CK Lam
- CK McPhee
- CL Buchheit
- CL Buchheit
- CL Buchheit
- CL Case
- Claudio Hetz
- CM Henry
- CN Casson
- Colin S. Duckett
- CP Baines
- CP Baines
- CP Dillon
- CP Dillon
- CP Dillon
- Cristina Muñoz-Pinedo
- CT Tan
- D Brenner
- D Brough
- D Chen
- D Crighton
- D Denton
- D Denton
- D Denton
- D Denton
- D Denton
- D Denton
- D Gatica
- D Goldschneider
- D Kranz
- D Li
- D Malin
- D Martin-Sanchez
- D Merino
- D Munoz-Espin
- D Piani
- D Ren
- D Stojkov
- D Tang
- D Tang
- D Vercammen
- D Vercammen
- D Wallach
- D Weaver
- D Yang
- DA Flusberg
- DA Rodriguez
- Daniel J. Klionsky
- Daolin Tang
- David C. Rubinsztein
- David M. Pereira
- David W. Andrews
- David Wallach
- DC Gray
- DH Cho
- Didac Carmona-Gutierrez
- Dieter Adam
- DJ Baker
- DJ Baker
- DJ Klionsky
- DJ McIlroy
- DL Berry
- DL Vaux
- DM Moquin
- DM Moujalled
- DM Pilla
- DM Rothwarf
- Domagoj Vucic
- Douglas R. Green
- DR Green
- DR Green
- DR Green
- DR Green
- DR Green
- DR Green
- DR Green
- DS Kempe
- DV Krysko
- E Arama
- E Basso
- E Buytaert
- E Candi
- E Fouquerel
- E Gavathiotis
- E Gavathiotis
- E Giampazolias
- E Kip
- E Lachaier
- E Lafont
- E Meunier
- E Perez
- E Vacchelli
- E Varfolomeev
- E Venereau
- E Zandi
- E Zandi
- EA Miao
- Edward A. Miao
- EF Lee
- EH Cheng
- EH Cheng
- EH Hinchcliffe
- EJ Park
- Eleonora Candi
- Eli Arama
- Emad S. Alnemri
- Emily H. Cheng
- Emre Sayan
- Enrico Lugli
- Eric H. Baehrecke
- Erwin F. Wagner
- Evripidis Gavathiotis
- EY Bassoy
- Eyal Gottlieb
- F Basit
- F Chalmin
- F Chen
- F Edlich
- F Ghiringhelli
- F Ke
- F Ke
- F Ke
- F Llambi
- F Llambi
- F Llambi
- F Loison
- F Madeo
- F Martin-Sanchez
- F McNab
- F Meitinger
- F Mille
- F Pietrocola
- F Todt
- F Wartha
- FB Chekeni
- FC Kischkel
- Feng Shao
- FK Chan
- FK Chan
- FL Scott
- FM Menzies
- FM Menzies
- FR Greten
- Francesca Bernassola
- Francesco Cecconi
- Francesco Di Virgilio
- Francis K.-M. Chan
- Frank Madeo
- G Brumatti
- G Casinelli
- G Denecker
- G Dewson
- G Droga-Mazovec
- G Ichim
- G Ichim
- G Kroemer
- G Kroemer
- G Kroemer
- G Monaco
- G Nunez
- G Quarato
- G Sun
- Gabriel A. Rabinovich
- Gabriel Nuñez
- Gerald M. Cohen
- Gerry Melino
- Gian Maria Fimia
- GO Latunde-Dada
- GP Sims
- GS Salvesen
- Guido Kroemer
- GW Dorn 2nd
- Gwenola Manic
- Gyorgy Hajnoczky
- Gyorgy Szabadkai
- H Appelqvist
- H Dai
- H Dai
- H Du
- H Hsu
- H Imai
- H Inoue
- H Inuzuka
- H Kazama
- H Kim
- H Kim
- H Li
- H Li
- H Otera
- H Parker
- H Puthalakath
- H Puthalakath
- H Sakahira
- H Wajant
- H Wang
- H Wang
- H Wang
- H Wang
- H Wang
- H Wang
- H Yang
- H Yang
- H Yuan
- H Yuan
- H Yuan
- H Zhang
- H Zhang
- HA Park
- Hamsa Puthalakath
- Hans-Uwe Simon
- HC Chen
- HE Kamber Kaya
- Henning Walczak
- Herbert W. Virgin
- Hidenori Ichijo
- Hinrich Gronemeyer
- HL Tang
- I Adkins
- I Amelio
- I Jaco
- I Jorgensen
- I Jorgensen
- I Jorgensen
- I Maejima
- I Martins
- I Marzo
- I Poursaitidis
- I Sturmlechner
- I Vitale
- I Vitale
- I Vitale
- I Vitale
- I Vitale
- I Vitale
- I Zanoni
- IC Low
- IE Dumitriu
- IE Gentle
- IE Wertz
- Ilio Vitale
- IP Nezis
- IP Nezis
- IR Powley
- Isaac S. Harris
- Ivano Amelio
- J Alanko
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- Y Li
- Y Li
- Y Liu
- Y Liu
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- Y Ma
- Y Ma
- Y Morizane
- Y Ou
- Y Pang
- Y Rong
- Y Shlyakhtina
- Y Subburaj
- Y Suzuki
- Y Tsujimoto
- Y Wang
- Y Wang
- Y Wang
- Y Wang
- Y Xie
- Y Xie
- Y Xie
- Y Zaltsman
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- YB Chen
- YC Hou
- YH Liao
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- Ying Wang
- YN Gong
- Yoshihide Tsujimoto
- YS Cho
- Yufang Shi
- Z Cai
- Z Cai
- Z Wang
- Z Wang
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- Z You
- Z Zhang
- Z Zhong
- Zahra Zakeri
- ZG Liu
- ZN Oltvai
- ZT Schafer
- ZX Chen
- ZX Chen
- Publication venue
- Cell Death Differ
- Publication date
- 01/01/2018
- Field of study
Over the past decade, the Nomenclature Committee on Cell Death (NCCD) has formulated guidelines for the definition and interpretation of cell death from morphological, biochemical, and functional perspectives. Since the field continues to expand and novel mechanisms that orchestrate multiple cell death pathways are unveiled, we propose an updated classification of cell death subroutines focusing on mechanistic and essential (as opposed to correlative and dispensable) aspects of the process. As we provide molecularly oriented definitions of terms including intrinsic apoptosis, extrinsic apoptosis, mitochondrial permeability transition (MPT)-driven necrosis, necroptosis, ferroptosis, pyroptosis, parthanatos, entotic cell death, NETotic cell death, lysosome-dependent cell death, autophagy-dependent cell death, immunogenic cell death, cellular senescence, and mitotic catastrophe, we discuss the utility of neologisms that refer to highly specialized instances of these processes. The mission of the NCCD is to provide a widely accepted nomenclature on cell death in support of the continued development of the field
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- Žerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
- Author
- A. -G. Wu
- A. C. Ma
- A. K. Au
- Abdel-Aziz A. K.
- Abdelfatah S.
- Abdellatif M.
- Abdoli A.
- Abel S.
- Abeliovich H.
- Abildgaard M. H.
- Abudu Y. P.
- Acevedo-Arozena A.
- Adamopoulos I. E.
- Adeli K.
- Adolph T. E.
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- Al-Gharaibeh A.
- Alaoui-Jamali M. A.
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- Zambelli V. O.
- Zanella I.
- Zang Q. S.
- Zanivan S.
- Zappavigna S.
- Zaragoza P.
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- Zarebkohan A.
- Zarrouk A.
- Zeitlin S. O.
- Zeng J.
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- Zheng G.
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- Zhivotovsky B.
- Zhong Q.
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- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
QOS-54USE OF CANNABINOIDS IN THE PEDIATRIC CENTRAL NERVOUS SYSTEM TUMOR POPULATION
- Author
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- Field of study
Safety and Feasibility of Outpatient Autologous Hematopoietic Stem Cell Transplantation in Pediatric Patients with Central Nervous System Tumors
- Publication venue
- 'American Society of Hematology'
- Publication date
- Field of study