Chemotherapeutic strategies that target irregularly produced or mutant proteins using monoclonal antibodies (mAbs) and tiny molecular inhibitors have been extensively employed to target cancer. However, because most intracellular proteins lack antigens or active sites with which mAbs or SMIs can engage, they have not been considered druggable targets. After extensive research, PROTACs (Proteolysis Targeting chimaeras) have become a promising way to work with proteins. Scaffolding proteins and transcription factors may also be targeted. The present targets of PROTACs include kinases like CDKs and RTKs, overexpressed oncogenic proteins like AR and BRDs, cancer-driven mutant proteins like EGFR, and disease-relevant fusion proteins like NPM/EML4-ALK and BCR-ABL. The inability of small-molecule intracellular degraders to enter cells and their low bioavailability can also be circumvented with PROTABs. The use of multispecific binding proteins is an improved way to target the breakdown of membrane-bound and cell-surface proteins.
Wong
S.Y.
Hynes
R.O.
Lymphatic or hematogenous dissemination: How does a metastatic tumor cell decide?
Cell Cycle2006
5
8
812
817
10.4161/cc.5.8.2646
16627996
Chen
Y.
Jin
J.
The application of ubiquitin ligases in the PROTAC drug design.
Acta Biochim. Biophys. Sin. (Shanghai)2020
52
7
776
790
10.1093/abbs/gmaa053
32506133
Liu
Z.
Hu
M.
Yang
Y.
Du
C.
Zhou
H.
Liu
C.
Chen
Y.
Fan
L.
Ma
H.
Gong
Y.
Xie
Y.
An overview of PROTACs: A promising drug discovery paradigm.
Mol. Biomed.2022
3
1
46
10.1186/s43556‑022‑00112‑0
36536188
Sakamoto
K.M.
Kim
K.B.
Kumagai
A.
Mercurio
F.
Crews
C.M.
Deshaies
R.J.
Protacs: Chimeric molecules that target proteins to the Skp1–Cullin–F box complex for ubiquitination and degradation.
Proc. Natl. Acad. Sci. USA2001
98
15
8554
8559
10.1073/pnas.141230798
11438690
Chvatal
S.A.
Logun
M.T.
Hayes
H.B.
Millard
D.C.
Karumbaiah
L.
Abstract 2187: Kinetics and potency of T Cell-mediated cytolysis of glioblastoma.
Cancer Res.2020
80
Suppl 16
2187
2187
10.1158/1538‑7445.AM2020‑2187
Daniels
T.R.
Bernabeu
E.
Rodríguez
J.A.
Patel
S.
Kozman
M.
Chiappetta
D.A.
Holler
E.
Ljubimova
J.Y.
Helguera
G.
Penichet
M.L.
The transferrin receptor and the targeted delivery of therapeutic agents against cancer.
Biochim. Biophys. Acta, Gen. Subj.2012
1820
3
291
317
10.1016/j.bbagen.2011.07.016
21851850
Huang
N.
Sun
X.
Li
P.
liu
X.
Zhang
X.
Chen
Q.
Xin
H.
TRIM family contribute to tumorigenesis, cancer development, and drug resistance.
Exp. Hematol. Oncol.2022
11
1
75
10.1186/s40164‑022‑00322‑w
36261847
Hershko
A.
The ubiquitin system for protein degradation and some of its roles in the control of the cell-division cycle (Nobel lecture).
Angew. Chem. Int. Ed.2005
44
37
5932
5943
10.1002/anie.200501724
16142823
Zhao
H.Y.
Xin
M.
Zhang
S.Q.
Progress of small molecules for targeted protein degradation: PROTACs and other technologies.
Drug Dev. Res.2023
84
2
337
394
10.1002/ddr.22026
36606428
Brien
G.L.
Remillard
D.
Shi
J.
Hemming
M.L.
Chabon
J.
Wynne
K.
Dillon
E.T.
Cagney
G.
Van Mierlo
G.
Baltissen
M.P.
Vermeulen
M.
Qi
J.
Fröhling
S.
Gray
N.S.
Bradner
J.E.
Vakoc
C.R.
Armstrong
S.A.
Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma.
eLife2018
7
e41305
10.7554/eLife.41305
30431433
Moreau
K.
Coen
M.
Zhang
A.X.
Pachl
F.
Castaldi
M.P.
Dahl
G.
Boyd
H.
Scott
C.
Newham
P.
Proteolysis‐targeting chimeras in drug development: A safety perspective.
Br. J. Pharmacol.2020
177
8
1709
1718
10.1111/bph.15014
32022252
Ishoey
M.
Chorn
S.
Singh
N.
Jaeger
M.G.
Brand
M.
Paulk
J.
Bauer
S.
Erb
M.A.
Parapatics
K.
Müller
A.C.
Bennett
K.L.
Ecker
G.F.
Bradner
J.E.
Winter
G.E.
Translation termination factor GSPT1 is a phenotypically relevant off-target of heterobifunctional phthalimide degraders.
ACS Chem. Biol.2018
13
3
553
560
10.1021/acschembio.7b00969
29356495
Vaid
A.
Gupta
A.
Momi
G.
Overall survival in stage IV EGFR mutation‑positive NSCLC: Comparing first‑, second‑ and third‑generation EGFR‑TKIs (Review).
Int. J. Oncol.2021
58
2
171
184
10.3892/ijo.2021.5168
33491758
Sitia
L.
Sevieri
M.
Signati
L.
Bonizzi
A.
Chesi
A.
Mainini
F.
Corsi
F.
Mazzucchelli
S.
HER-2-targeted nanoparticles for breast cancer diagnosis and treatment.
Cancers (Basel)2022
14
10
2424
10.3390/cancers14102424
35626028
Xue
G.
Wang
K.
Zhou
D.
Zhong
H.
Pan
Z.
Light-induced protein degradation with photocaged PROTACs.
J. Am. Chem. Soc.2019
141
46
18370
18374
10.1021/jacs.9b06422
31566962
Liu
J.
Chen
H.
Ma
L.
He
Z.
Wang
D.
Liu
Y.
Lin
Q.
Zhang
T.
Gray
N.
Kaniskan
H.Ü.
Jin
J.
Wei
W.
Light-induced control of protein destruction by opto-PROTAC.
Sci. Adv.2020
6
8
eaay5154
10.1126/sciadv.aay5154
32128407
Naro
Y.
Darrah
K.
Deiters
A.
Optical control of small molecule-induced protein degradation.
J. Am. Chem. Soc.2020
142
5
2193
2197
10.1021/jacs.9b12718
31927988
Reynders
M.
Matsuura
B.S.
Bérouti
M.
Simoneschi
D.
Marzio
A.
Pagano
M.
Trauner
D.
PHOTACs enable optical control of protein degradation.
Sci. Adv.2020
6
8
eaay5064
10.1126/sciadv.aay5064
32128406
Pfaff
P.
Samarasinghe
K.T.G.
Crews
C.M.
Carreira
E.M.
Reversible spatiotemporal control of induced protein degradation by bistable PhotoPROTACs.
ACS Cent. Sci.2019
5
10
1682
1690
10.1021/acscentsci.9b00713
31660436
Salami
J.
Alabi
S.
Willard
R.R.
Vitale
N.J.
Wang
J.
Dong
H.
Jin
M.
McDonnell
D.P.
Crew
A.P.
Neklesa
T.K.
Crews
C.M.
Androgen receptor degradation by the proteolysis-targeting chimera ARCC-4 outperforms enzalutamide in cellular models of prostate cancer drug resistance.
Commun. Biol.2018
1
1
100
10.1038/s42003‑018‑0105‑8
30271980
Petrylak
D.P.
Gao
X.
Vogelzang
N.J.
Garfield
M.H.
Taylor
I.
Dougan Moore
M.
Peck
R.A.
Burris
H.A.
First-in-human phase I study of ARV-110, an androgen receptor (AR) PROTAC degrader in patients (pts) with metastatic castrate-resistant prostate cancer (mCRPC) following enzalutamide (ENZ) and/or abiraterone (ABI).
J. Clin. Oncol.2020
38
Suppl 15
3500
3500
10.1200/JCO.2020.38.15_suppl.3500
Rugo
H.S.
Bardia
A.
Tolaney
S.M.
Arteaga
C.
Cortes
J.
Sohn
J.
Marmé
F.
Hong
Q.
Delaney
R.J.
Hafeez
A.
André
F.
Schmid
P.
TROPiCS-02: A Phase III study investigating sacituzumab govitecan in the treatment of HR+/HER2- metastatic breast cancer.
Future Oncol.2020
16
12
705
715
10.2217/fon‑2020‑0163
32223649
Bondeson
D.P.
Mares
A.
Smith
I.E.D.
Ko
E.
Campos
S.
Miah
A.H.
Mulholland
K.E.
Routly
N.
Buckley
D.L.
Gustafson
J.L.
Zinn
N.
Grandi
P.
Shimamura
S.
Bergamini
G.
Faelth-Savitski
M.
Bantscheff
M.
Cox
C.
Gordon
D.A.
Willard
R.R.
Flanagan
J.J.
Casillas
L.N.
Votta
B.J.
den Besten
W.
Famm
K.
Kruidenier
L.
Carter
P.S.
Harling
J.D.
Churcher
I.
Crews
C.M.
Catalytic in vivo protein knockdown by small-molecule PROTACs.
Nat. Chem. Biol.2015
11
8
611
617
10.1038/nchembio.1858
26075522
Winter
C.
Nilsson
M.P.
Olsson
E.
George
A.M.
Chen
Y.
Kvist
A.
Törngren
T.
Vallon-Christersson
J.
Hegardt
C.
Häkkinen
J.
Jönsson
G.
Grabau
D.
Malmberg
M.
Kristoffersson
U.
Rehn
M.
Gruvberger-Saal
S.K.
Larsson
C.
Borg
Å.
Loman
N.
Saal
L.H.
Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic.
Ann. Oncol.2016
27
8
1532
1538
10.1093/annonc/mdw209
27194814
Fitzmaurice
C.
Abate
D.
Abbasi
N.
Abbastabar
H.
Abd-Allah
F.
Abdel-Rahman
O.
Abdelalim
A.
Abdoli
A.
Abdollahpour
I.
Abdulle
A.S.M.
Abebe
N.D.
Abraha
H.N.
Abu-Raddad
L.J.
Abualhasan
A.
Adedeji
I.A.
Advani
S.M.
Afarideh
M.
Afshari
M.
Aghaali
M.
Agius
D.
Agrawal
S.
Ahmadi
A.
Ahmadian
E.
Ahmadpour
E.
Ahmed
M.B.
Akbari
M.E.
Akinyemiju
T.
Al-Aly
Z.
AlAbdulKader
A.M.
Alahdab
F.
Alam
T.
Alamene
G.M.
Alemnew
B.T.T.
Alene
K.A.
Alinia
C.
Alipour
V.
Aljunid
S.M.
Bakeshei
F.A.
Almadi
M.A.H.
Almasi-Hashiani
A.
Alsharif
U.
Alsowaidi
S.
Alvis-Guzman
N.
Amini
E.
Amini
S.
Amoako
Y.A.
Anbari
Z.
Anber
N.H.
Andrei
C.L.
Anjomshoa
M.
Ansari
F.
Ansariadi
A.
Appiah
S.C.Y.
Arab-Zozani
M.
Arabloo
J.
Arefi
Z.
Aremu
O.
Areri
H.A.
Artaman
A.
Asayesh
H.
Asfaw
E.T.
Ashagre
A.F.
Assadi
R.
Ataeinia
B.
Atalay
H.T.
Ataro
Z.
Atique
S.
Ausloos
M.
Avila-Burgos
L.
Avokpaho
E.F.G.A.
Awasthi
A.
Awoke
N.
Ayala Quintanilla
B.P.
Ayanore
M.A.
Ayele
H.T.
Babaee
E.
Bacha
U.
Badawi
A.
Bagherzadeh
M.
Bagli
E.
Balakrishnan
S.
Balouchi
A.
Bärnighausen
T.W.
Battista
R.J.
Behzadifar
M.
Behzadifar
M.
Bekele
B.B.
Belay
Y.B.
Belayneh
Y.M.
Berfield
K.K.S.
Berhane
A.
Bernabe
E.
Beuran
M.
Bhakta
N.
Bhattacharyya
K.
Biadgo
B.
Bijani
A.
Bin Sayeed
M.S.
Birungi
C.
Bisignano
C.
Bitew
H.
Bjørge
T.
Bleyer
A.
Bogale
K.A.
Bojia
H.A.
Borzì
A.M.
Bosetti
C.
Bou-Orm
I.R.
Brenner
H.
Brewer
J.D.
Briko
A.N.
Briko
N.I.
Bustamante-Teixeira
M.T.
Butt
Z.A.
Carreras
G.
Carrero
J.J.
Carvalho
F.
Castro
C.
Castro
F.
Catalá-López
F.
Cerin
E.
Chaiah
Y.
Chanie
W.F.
Chattu
V.K.
Chaturvedi
P.
Chauhan
N.S.
Chehrazi
M.
Chiang
P.P.C.
Chichiabellu
T.Y.
Chido-Amajuoyi
O.G.
Chimed-Ochir
O.
Choi
J.Y.J.
Christopher
D.J.
Chu
D.T.
Constantin
M.M.
Costa
V.M.
Crocetti
E.
Crowe
C.S.
Curado
M.P.
Dahlawi
S.M.A.
Damiani
G.
Darwish
A.H.
Daryani
A.
das Neves
J.
Demeke
F.M.
Demis
A.B.
Demissie
B.W.
Demoz
G.T.
Denova-Gutiérrez
E.
Derakhshani
A.
Deribe
K.S.
Desai
R.
Desalegn
B.B.
Desta
M.
Dey
S.
Dharmaratne
S.D.
Dhimal
M.
Diaz
D.
Dinberu
M.T.T.
Djalalinia
S.
Doku
D.T.
Drake
T.M.
Dubey
M.
Dubljanin
E.
Duken
E.E.
Ebrahimi
H.
Effiong
A.
Eftekhari
A.
El Sayed
I.
Zaki
M.E.S.
El-Jaafary
S.I.
El-Khatib
Z.
Elemineh
D.A.
Elkout
H.
Ellenbogen
R.G.
Elsharkawy
A.
Emamian
M.H.
Endalew
D.A.
Endries
A.Y.
Eshrati
B.
Fadhil
I.
Fallah Omrani
V.
Faramarzi
M.
Farhangi
M.A.
Farioli
A.
Farzadfar
F.
Fentahun
N.
Fernandes
E.
Feyissa
G.T.
Filip
I.
Fischer
F.
Fisher
J.L.
Force
L.M.
Foroutan
M.
Freitas
M.
Fukumoto
T.
Futran
N.D.
Gallus
S.
Gankpe
F.G.
Gayesa
R.T.
Gebrehiwot
T.T.
Gebremeskel
G.G.
Gedefaw
G.A.
Gelaw
B.K.
Geta
B.
Getachew
S.
Gezae
K.E.
Ghafourifard
M.
Ghajar
A.
Ghashghaee
A.
Gholamian
A.
Gill
P.S.
Ginindza
T.T.G.
Girmay
A.
Gizaw
M.
Gomez
R.S.
Gopalani
S.V.
Gorini
G.
Goulart
B.N.G.
Grada
A.
Ribeiro Guerra
M.
Guimaraes
A.L.S.
Gupta
P.C.
Gupta
R.
Hadkhale
K.
Haj-Mirzaian
A.
Haj-Mirzaian
A.
Hamadeh
R.R.
Hamidi
S.
Hanfore
L.K.
Haro
J.M.
Hasankhani
M.
Hasanzadeh
A.
Hassen
H.Y.
Hay
R.J.
Hay
S.I.
Henok
A.
Henry
N.J.
Herteliu
C.
Hidru
H.D.
Hoang
C.L.
Hole
M.K.
Hoogar
P.
Horita
N.
Hosgood
H.D.
Hosseini
M.
Hosseinzadeh
M.
Hostiuc
M.
Hostiuc
S.
Househ
M.
Hussen
M.M.
Ileanu
B.
Ilic
M.D.
Innos
K.
Irvani
S.S.N.
Iseh
K.R.
Islam
S.M.S.
Islami
F.
Jafari Balalami
N.
Jafarinia
M.
Jahangiry
L.
Jahani
M.A.
Jahanmehr
N.
Jakovljevic
M.
James
S.L.
Javanbakht
M.
Jayaraman
S.
Jee
S.H.
Jenabi
E.
Jha
R.P.
Jonas
J.B.
Jonnagaddala
J.
Joo
T.
Jungari
S.B.
Jürisson
M.
Kabir
A.
Kamangar
F.
Karch
A.
Karimi
N.
Karimian
A.
Kasaeian
A.
Kasahun
G.G.
Kassa
B.
Kassa
T.D.
Kassaw
M.W.
Kaul
A.
Keiyoro
P.N.
Kelbore
A.G.
Kerbo
A.A.
Khader
Y.S.
Khalilarjmandi
M.
Khan
E.A.
Khan
G.
Khang
Y.H.
Khatab
K.
Khater
A.
Khayamzadeh
M.
Khazaee-Pool
M.
Khazaei
S.
Khoja
A.T.
Khosravi
M.H.
Khubchandani
J.
Kianipour
N.
Kim
D.
Kim
Y.J.
Kisa
A.
Kisa
S.
Kissimova-Skarbek
K.
Komaki
H.
Koyanagi
A.
Krohn
K.J.
Bicer
B.K.
Kugbey
N.
Kumar
V.
Kuupiel
D.
La Vecchia
C.
Lad
D.P.
Lake
E.A.
Lakew
A.M.
Lal
D.K.
Lami
F.H.
Lan
Q.
Lasrado
S.
Lauriola
P.
Lazarus
J.V.
Leigh
J.
Leshargie
C.T.
Liao
Y.
Limenih
M.A.
Listl
S.
Lopez
A.D.
Lopukhov
P.D.
Lunevicius
R.
Madadin
M.
Magdeldin
S.
El Razek
H.M.A.
Majeed
A.
Maleki
A.
Malekzadeh
R.
Manafi
A.
Manafi
N.
Manamo
W.A.
Mansourian
M.
Mansournia
M.A.
Mantovani
L.G.
Maroufizadeh
S.
Martini
S.M.S.
Mashamba-Thompson
T.P.
Massenburg
B.B.
Maswabi
M.T.
Mathur
M.R.
McAlinden
C.
McKee
M.
Meheretu
H.A.A.
Mehrotra
R.
Mehta
V.
Meier
T.
Melaku
Y.A.
Meles
G.G.
Meles
H.G.
Melese
A.
Melku
M.
Memiah
P.T.N.
Mendoza
W.
Menezes
R.G.
Merat
S.
Meretoja
T.J.
Mestrovic
T.
Miazgowski
B.
Miazgowski
T.
Mihretie
K.M.M.
Miller
T.R.
Mills
E.J.
Mir
S.M.
Mirzaei
H.
Mirzaei
H.R.
Mishra
R.
Moazen
B.
Mohammad
D.K.
Mohammad
K.A.
Mohammad
Y.
Darwesh
A.M.
Mohammadbeigi
A.
Mohammadi
H.
Mohammadi
M.
Mohammadian
M.
Mohammadian-Hafshejani
A.
Mohammadoo-Khorasani
M.
Mohammadpourhodki
R.
Mohammed
A.S.
Mohammed
J.A.
Mohammed
S.
Mohebi
F.
Mokdad
A.H.
Monasta
L.
Moodley
Y.
Moosazadeh
M.
Moossavi
M.
Moradi
G.
Moradi-Joo
M.
Moradi-Lakeh
M.
Moradpour
F.
Morawska
L.
Morgado-da-Costa
J.
Morisaki
N.
Morrison
S.D.
Mosapour
A.
Mousavi
S.M.
Muche
A.A.
Muhammed
O.S.S.
Musa
J.
Nabhan
A.F.
Naderi
M.
Nagarajan
A.J.
Nagel
G.
Nahvijou
A.
Naik
G.
Najafi
F.
Naldi
L.
Nam
H.S.
Nasiri
N.
Nazari
J.
Negoi
I.
Neupane
S.
Newcomb
P.A.
Nggada
H.A.
Ngunjiri
J.W.
Nguyen
C.T.
Nikniaz
L.
Ningrum
D.N.A.
Nirayo
Y.L.
Nixon
M.R.
Nnaji
C.A.
Nojomi
M.
Nosratnejad
S.
Shiadeh
M.N.
Obsa
M.S.
Ofori-Asenso
R.
Ogbo
F.A.
Oh
I.H.
Olagunju
A.T.
Olagunju
T.O.
Oluwasanu
M.M.
Omonisi
A.E.
Onwujekwe
O.E.
Oommen
A.M.
Oren
E.
Ortega-Altamirano
D.D.V.
Ota
E.
Otstavnov
S.S.
Owolabi
M.O.
P A
M.
Padubidri
J.R.
Pakhale
S.
Pakpour
A.H.
Pana
A.
Park
E.K.
Parsian
H.
Pashaei
T.
Patel
S.
Patil
S.T.
Pennini
A.
Pereira
D.M.
Piccinelli
C.
Pillay
J.D.
Pirestani
M.
Pishgar
F.
Postma
M.J.
Pourjafar
H.
Pourmalek
F.
Pourshams
A.
Prakash
S.
Prasad
N.
Qorbani
M.
Rabiee
M.
Rabiee
N.
Radfar
A.
Rafiei
A.
Rahim
F.
Rahimi
M.
Rahman
M.A.
Rajati
F.
Rana
S.M.
Raoofi
S.
Rath
G.K.
Rawaf
D.L.
Rawaf
S.
Reiner
R.C.
Renzaho
A.M.N.
Rezaei
N.
Rezapour
A.
Ribeiro
A.I.
Ribeiro
D.
Ronfani
L.
Roro
E.M.
Roshandel
G.
Rostami
A.
Saad
R.S.
Sabbagh
P.
Sabour
S.
Saddik
B.
Safiri
S.
Sahebkar
A.
Salahshoor
M.R.
Salehi
F.
Salem
H.
Salem
M.R.
Salimzadeh
H.
Salomon
J.A.
Samy
A.M.
Sanabria
J.
Santric Milicevic
M.M.
Sartorius
B.
Sarveazad
A.
Sathian
B.
Satpathy
M.
Savic
M.
Sawhney
M.
Sayyah
M.
Schneider
I.J.C.
Schöttker
B.
Sekerija
M.
Sepanlou
S.G.
Sepehrimanesh
M.
Seyedmousavi
S.
Shaahmadi
F.
Shabaninejad
H.
Shahbaz
M.
Shaikh
M.A.
Shamshirian
A.
Shamsizadeh
M.
Sharafi
H.
Sharafi
Z.
Sharif
M.
Sharifi
A.
Sharifi
H.
Sharma
R.
Sheikh
A.
Shirkoohi
R.
Shukla
S.R.
Si
S.
Siabani
S.
Silva
D.A.S.
Silveira
D.G.A.
Singh
A.
Singh
J.A.
Sisay
S.
Sitas
F.
Sobngwi
E.
Soofi
M.
Soriano
J.B.
Stathopoulou
V.
Sufiyan
M.B.
Tabarés-Seisdedos
R.
Tabuchi
T.
Takahashi
K.
Tamtaji
O.R.
Tarawneh
M.R.
Tassew
S.G.
Taymoori
P.
Tehrani-Banihashemi
A.
Temsah
M.H.
Temsah
O.
Tesfay
B.E.
Tesfay
F.H.
Teshale
M.Y.
Tessema
G.A.
Thapa
S.
Tlaye
K.G.
Topor-Madry
R.
Tovani-Palone
M.R.
Traini
E.
Tran
B.X.
Tran
K.B.
Tsadik
A.G.
Ullah
I.
Uthman
O.A.
Vacante
M.
Vaezi
M.
Varona Pérez
P.
Veisani
Y.
Vidale
S.
Violante
F.S.
Vlassov
V.
Vollset
S.E.
Vos
T.
Vosoughi
K.
Vu
G.T.
Vujcic
I.S.
Wabinga
H.
Wachamo
T.M.
Wagnew
F.S.
Waheed
Y.
Weldegebreal
F.
Weldesamuel
G.T.
Wijeratne
T.
Wondafrash
D.Z.
Wonde
T.E.
Wondmieneh
A.B.
Workie
H.M.
Yadav
R.
Yadegar
A.
Yadollahpour
A.
Yaseri
M.
Yazdi-Feyzabadi
V.
Yeshaneh
A.
Yimam
M.A.
Yimer
E.M.
Yisma
E.
Yonemoto
N.
Younis
M.Z.
Yousefi
B.
Yousefifard
M.
Yu
C.
Zabeh
E.
Zadnik
V.
Moghadam
T.Z.
Zaidi
Z.
Zamani
M.
Zandian
H.
Zangeneh
A.
Zaki
L.
Zendehdel
K.
Zenebe
Z.M.
Zewale
T.A.
Ziapour
A.
Zodpey
S.
Murray
C.J.L.
Global, regional, and national cancer incidence, mortality, years of life lost, years lived with disability, and disability-adjusted life-years for 29 cancer groups, 1990 to 2017.
JAMA Oncol.2019
5
12
1749
1768
10.1001/jamaoncol.2019.2996
31560378
Ruiz-Saenz
A.
Dreyer
C.
Campbell
M.R.
Steri
V.
Gulizia
N.
Moasser
M.M.
HER2 amplification in tumors activates PI3K/Akt signaling independent of HER3.
Cancer Res.2018
78
13
3645
3658
10.1158/0008‑5472.CAN‑18‑0430
29760043
Wang
W.
Yang
J.
Liao
Y.Y.
Cheng
G.
Chen
J.
Mo
S.
Yuan
L.
Cheng
X.D.
Qin
J.J.
Shao
Z.
Aspeterreurone A, a cytotoxic dihydrobenzofuran–phenyl acrylate hybrid from the deep-sea-derived fungus Aspergillus terreus CC-S06-18.
J. Nat. Prod.2020
83
6
1998
2003
10.1021/acs.jnatprod.0c00189
32489099
Nowak
R.P.
DeAngelo
S.L.
Buckley
D.
He
Z.
Donovan
K.A.
An
J.
Safaee
N.
Jedrychowski
M.P.
Ponthier
C.M.
Ishoey
M.
Zhang
T.
Mancias
J.D.
Gray
N.S.
Bradner
J.E.
Fischer
E.S.
Plasticity in binding confers selectivity in ligand-induced protein degradation.
Nat. Chem. Biol.2018
14
7
706
714
10.1038/s41589‑018‑0055‑y
29892083
Kaefer
A.
Yang
J.
Noertersheuser
P.
Mensing
S.
Humerickhouse
R.
Awni
W.
Xiong
H.
Mechanism-based pharmacokinetic/pharmacodynamic meta-analysis of navitoclax (ABT-263) induced thrombocytopenia.
Cancer Chemother. Pharmacol.2014
74
3
593
602
10.1007/s00280‑014‑2530‑9
25053389
Zhu
H.
Wang
J.
Zhang
Q.
Pan
X.
Zhang
J.
Novel strategies and promising opportunities for targeted protein degradation: An innovative therapeutic approach to overcome cancer resistance.
Pharmacol. Ther.2023
244
108371
10.1016/j.pharmthera.2023.108371
36871783
Fan
R.
Tao
X.
Zhai
X.
Zhu
Y.
Li
Y.
Chen
Y.
Dong
D.
Yang
S.
Lv
L.
Application of aptamer-drug delivery system in the therapy of breast cancer.
Biomed. Pharmacother.2023
161
114444
10.1016/j.biopha.2023.114444
36857912
Kumar Deshmukh
F.
Yaffe
D.
Olshina
M.
Ben-Nissan
G.
Sharon
M.
The contribution of the 20S proteasome to proteostasis.
Biomolecules2019
9
5
190
10.3390/biom9050190
31100951
Flanagan
J.
Qian
Y.
Gough
S.
Andreoli
M.
Bookbinder
M.
Cadelina
G.
2019
Abstract P5-04-18: ARV-471, an oral estrogen receptor PROTAC degrader for breast cancer.
Cancer Res.
79
Suppl 4
P5-04-18
10.1158/1538‑7445.SABCS18‑P5‑04‑18
Bond
M.J.
Chu
L.
Nalawansha
D.A.
Li
K.
Crews
C.M.
Targeted degradation of oncogenic KRAS G12C by VHL-recruiting PROTACs.
ACS Cent. Sci.2020
6
8
1367
1375
10.1021/acscentsci.0c00411
32875077
Egorova
E.A.
Nikitin
M.P.
Delivery of theranostic nanoparticles to various cancers by means of integrin-binding peptides.
Int. J. Mol. Sci.2022
23
22
13735
10.3390/ijms232213735
36430214
Benn
J.A.
Mukadam
A.S.
McEwan
W.A.
Targeted protein degradation using intracellular antibodies and its application to neurodegenerative disease.
Semin. Cell Dev. Biol.2022
126
138
149
10.1016/j.semcdb.2021.09.012
34654628
Hochstrasser
M.
Ubiquitin, proteasomes, and the regulation of intracellular protein degradation.
Curr. Opin. Cell Biol.1995
7
2
215
223
10.1016/0955‑0674(95)80031‑X
7612274
Foss
S.
Watkinson
R.
Sandlie
I.
James
L.C.
Andersen
J.T.
TRIM 21: A cytosolic Fc receptor with broad antibody isotype specificity.
Immunol. Rev.2015
268
1
328
339
10.1111/imr.12363
26497531
Li
R.
Liu
M.
Yang
Z.
Li
J.
Gao
Y.
Tan
R.
Proteolysis-targeting chimeras (PROTACs) in cancer therapy: Present and future.
Molecules2022
27
24
8828
10.3390/molecules27248828
36557960
Vivancos
Á.
Segarra
C.
Albrecht
M.
Mesoionic and related less heteroatom-stabilized N-heterocyclic carbene complexes: Synthesis, catalysis, and other applications.
Chem. Rev.2018
118
19
9493
9586
10.1021/acs.chemrev.8b00148
30014699
Nguyen
T.T.L.
Kim
J.W.
Choi
H.I.
Maeng
H.J.
Koo
T.S.
Development of an LC-MS/MS method for aRV-110, a PROTAC molecule, and applications to pharmacokinetic studies.
Molecules2022
27
6
1977
10.3390/molecules27061977
35335338
Zorba
A.
Nguyen
C.
Xu
Y.
Starr
J.
Borzilleri
K.
Smith
J.
Zhu
H.
Farley
K.A.
Ding
W.
Schiemer
J.
Feng
X.
Chang
J.S.
Uccello
D.P.
Young
J.A.
Garcia-Irrizary
C.N.
Czabaniuk
L.
Schuff
B.
Oliver
R.
Montgomery
J.
Hayward
M.M.
Coe
J.
Chen
J.
Niosi
M.
Luthra
S.
Shah
J.C.
El-Kattan
A.
Qiu
X.
West
G.M.
Noe
M.C.
Shanmugasundaram
V.
Gilbert
A.M.
Brown
M.F.
Calabrese
M.F.
Delineating the role of cooperativity in the design of potent PROTACs for BTK.
Proc. Natl. Acad. Sci. USA2018
115
31
E7285
E7292
10.1073/pnas.1803662115
30012605
Burslem
G.M.
Smith
B.E.
Lai
A.C.
Jaime-Figueroa
S.
McQuaid
D.C.
Bondeson
D.P.
Toure
M.
Dong
H.
Qian
Y.
Wang
J.
Crew
A.P.
Hines
J.
Crews
C.M.
The advantages of targeted protein degradation over inhibition: An RTK case study.
Cell Chem. Biol.2018
25
1
67
77.e3
10.1016/j.chembiol.2017.09.009
29129716
Qu
M.H.
Zeng
R.F.
Fang
S.
Dai
Q.S.
Li
H.P.
Long
J.T.
Liposome-based co-delivery of siRNA and docetaxel for the synergistic treatment of lung cancer.
Int. J. Pharm.2014
474
1-2
112
122
10.1016/j.ijpharm.2014.08.019
25138252
Dristant
U.
Mukherjee
K.
Saha
S.
Maity
D.
RETRACTED: An overview of polymeric nanoparticles-based drug delivery system in cancer treatment.
Technol. Cancer Res. Treat.2023
22
15330338231152083
10.1177/15330338231152083
36718541
Zhang
R.X.
Cai
P.
Zhang
T.
Chen
K.
Li
J.
Cheng
J.
Pang
K.S.
Adissu
H.A.
Rauth
A.M.
Wu
X.Y.
Polymer–lipid hybrid nanoparticles synchronize pharmacokinetics of co-encapsulated doxorubicin–mitomycin C and enable their spatiotemporal co-delivery and local bioavailability in breast tumor.
Nanomedicine2016
12
5
1279
1290
10.1016/j.nano.2015.12.383
26772427
Lu
G.
Wang
X.
Li
F.
Wang
S.
Zhao
J.
Wang
J.
Liu
J.
Lyu
C.
Ye
P.
Tan
H.
Li
W.
Ma
G.
Wei
W.
Engineered biomimetic nanoparticles achieve targeted delivery and efficient metabolism-based synergistic therapy against glioblastoma.
Nat. Commun.2022
13
1
4214
10.1038/s41467‑022‑31799‑y
35864093
Zhou
R.
Zhang
M.
Xi
J.
Li
J.
Ma
R.
Ren
L.
Bai
Z.
Qi
K.
Li
X.
Gold nanorods-based photothermal therapy: Interactions between biostructure, nanomaterial, and near-infrared irradiation.
Nanoscale Res. Lett.2022
17
1
68
10.1186/s11671‑022‑03706‑3
35882718
Cavallaro
G.
Sardo
C.
Craparo
E.F.
Porsio
B.
Giammona
G.
Polymeric nanoparticles for siRNA delivery: Production and applications.
Int. J. Pharm.2017
525
2
313
333
10.1016/j.ijpharm.2017.04.008
28416401
Cheng
Y.
Jiao
X.
Fan
W.
Yang
Z.
Wen
Y.
Chen
X.
Controllable synthesis of versatile mesoporous organosilica nanoparticles as precision cancer theranostics.
Biomaterials2020
256
120191
10.1016/j.biomaterials.2020.120191
32593907
Beh
C.W.
Seow
W.Y.
Wang
Y.
Zhang
Y.
Ong
Z.Y.
Ee
P.L.R.
Yang
Y.Y.
Efficient delivery of Bcl-2-targeted siRNA using cationic polymer nanoparticles: Downregulating mRNA expression level and sensitizing cancer cells to anticancer drug.
Biomacromolecules2009
10
1
41
48
10.1021/bm801109g
19072631
Talaei
S.
Mellatyar
H.
Asadi
A.
Akbarzadeh
A.
Sheervalilou
R.
Zarghami
N.
Spotlight on 17‐AAG as an Hsp90 inhibitor for molecular targeted cancer treatment.
Chem. Biol. Drug Des.2019
93
5
760
786
10.1111/cbdd.13486
30697932