Proteomics technologies for cancer liquid biopsies

被引:117
作者
Ding, Zhiyong [1 ]
Wang, Nan [1 ]
Ji, Ning [2 ,3 ]
Chen, Zhe-Sheng [2 ]
机构
[1] Fynn Biotechnol Ltd, Mills Inst Personalized Canc Care, High Tech & Innovat Zone, Gangxing 3rd Rd,Bldg 2,Rm 2201, Jinan 250101, Shandong, Peoples R China
[2] St Johns Univ, Inst Biotechnol, Dept Pharmaceut Sci, Coll Pharm & Hlth Sci, 8000 Utopia Pkwy, Queens, NY 11439 USA
[3] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Tianjins Clin Res Ctr Canc, Key Lab Canc Prevent & Therapy, Tianjin 300060, Peoples R China
关键词
Proteomics; Cancer liquid biopsy; Aptamer; Proximity extension assay (PEA); Reverse phase protein arrays (RPPA); Mass spectrometry (MS); Antibody arrays; PHASE PROTEIN ARRAY; ANTIBODY ARRAYS; BIOMARKER DISCOVERY; PLASMA PROTEOME; LUNG-CANCER; VALIDATION; IDENTIFICATION; MICROARRAYS; UTILITY; MARKER;
D O I
10.1186/s12943-022-01526-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alterations in DNAs could not reveal what happened in proteins. The accumulated alterations of DNAs would change the manifestation of proteins. Therefore, as is the case in cancer liquid biopsies, deep proteome profiling will likely provide invaluable and clinically relevant information in real-time throughout all stages of cancer progression. However, due to the great complexity of proteomes in liquid biopsy samples and the limitations of proteomic technologies compared to high-plex sequencing technologies, proteomic discoveries have yet lagged behind their counterpart, genomic technologies. Therefore, novel protein technologies are in urgent demand to fulfill the goals set out for biomarker discovery in cancer liquid biopsies. Notably, conventional and innovative technologies are being rapidly developed for proteomic analysis in cancer liquid biopsies. These advances have greatly facilitated early detection, diagnosis, prognosis, and monitoring of cancer evolution, adapted or adopted in response to therapeutic interventions. In this paper, we review the high-plex proteomics technologies that are capable of measuring at least hundreds of proteins simultaneously from liquid biopsy samples, ranging from traditional technologies based on mass spectrometry (MS) and antibody/antigen arrays to innovative technologies based on aptamer, proximity extension assay (PEA), and reverse phase protein arrays (RPPA).
引用
收藏
页数:11
相关论文
共 83 条
  • [1] Potential early clinical stage colorectal cancer diagnosis using a proteomics blood test panel
    Ahn, Seong Beom
    Sharma, Samridhi
    Mohamedali, Abidali
    Mahboob, Sadia
    Redmond, William J.
    Pascovici, Dana
    Wu, Jemma X.
    Zaw, Thin
    Adhikari, Subash
    Vaibhav, Vineet
    Nice, Edouard C.
    Baker, Mark S.
    [J]. CLINICAL PROTEOMICS, 2019, 16 (01)
  • [2] Realizing the Promise of Reverse Phase Protein Arrays for Clinical, Translational, and Basic Research: A Workshop Report
    Akbani, Rehan
    Becker, Karl-Friedrich
    Carragher, Neil
    Goldstein, Ted
    de Koning, Leanne
    Korf, Ulrike
    Liotta, Lance
    Mills, Gordon B.
    Nishizuka, Satoshi S.
    Pawlak, Michael
    Petricoin, Emanuel F.
    Pollard, Harvey B.
    Serrels, Bryan
    Zhu, Jingchun
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2014, 13 (07) : 1625 - 1643
  • [3] Liquid Biopsy: From Discovery to Clinical Application
    Alix-Panabieres, Catherine
    Pantel, Klaus
    [J]. CANCER DISCOVERY, 2021, 11 (04) : 858 - 873
  • [4] Liquid biopsies and cancer omics
    Amelio, Ivano
    Bertolo, Riccardo
    Bove, Pierluigi
    Buonomo, Oreste Claudio
    Candi, Eleonora
    Chiocchi, Marcello
    Cipriani, Chiara
    Di Daniele, Nicola
    Ganini, Carlo
    Juhl, Hartmut
    Mauriello, Alessandro
    Marani, Carla
    Marshall, John
    Montanaro, Manuela
    Palmieri, Giampiero
    Piacentini, Mauro
    Sica, Giuseppe
    Tesauro, Manfredi
    Rovella, Valentina
    Tisone, Giuseppe
    Shi, Yufang
    Wang, Ying
    Melino, Gerry
    [J]. CELL DEATH DISCOVERY, 2020, 6 (01)
  • [5] The human plasma proteome - A nonredundant list developed by combination of four separate sources
    Anderson, NL
    Polanski, M
    Pieper, R
    Gatlin, T
    Tirumalai, RS
    Conrads, TP
    Veenstra, TD
    Adkins, JN
    Pounds, JG
    Fagan, R
    Lobley, A
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2004, 3 (04) : 311 - 326
  • [6] Homogenous 96-Plex PEA Immunoassay Exhibiting High Sensitivity, Specificity, and Excellent Scalability
    Assarsson, Erika
    Lundberg, Martin
    Holmquist, Goeran
    Bjoerkesten, Johan
    Thorsen, Stine Bucht
    Ekman, Daniel
    Eriksson, Anna
    Dickens, Emma Rennel
    Ohlsson, Sandra
    Edfeldt, Gabriella
    Andersson, Ann-Catrin
    Lindstedt, Patrik
    Stenvang, Jan
    Gullberg, Mats
    Fredriksson, Simon
    [J]. PLOS ONE, 2014, 9 (04):
  • [7] Biomarkers and Strategies for Early Detection of Ovarian Cancer
    Bast, Robert C., Jr.
    Lu, Zhen
    Han, Chae Young
    Lu, Karen H.
    Anderson, Karen S.
    Drescher, Charles W.
    Skates, Steven J.
    [J]. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2020, 29 (12) : 2504 - 2512
  • [8] Identification of Candidate Plasma Protein Biomarkers for Cervical Cancer Using the Multiplex Proximity Extension Assay
    Berggrund, Malin
    Enroth, Stefan
    Lundberg, Martin
    Assarsson, Erika
    Stalberg, Karin
    Lindquist, David
    Hallmans, Goran
    Grankvist, Kjeii
    Olovsson, Matts
    Gyllensten, Ulf
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2019, 18 (04) : 735 - 743
  • [9] Evaluation and Validation of Plasma Proteins Using Two Different Protein Detection Methods for Early Detection of Colorectal Cancer
    Bhardwaj, Megha
    Gies, Anton
    Weigl, Korbinian
    Tikk, Kaja
    Benner, Axel
    Schrotz-King, Petra
    Borchers, Christoph H.
    Brenner, Hermann
    [J]. CANCERS, 2019, 11 (10)
  • [10] Challenges and Opportunities in Clinical Applications of Blood-Based Proteomics in Cancer
    Bhawal, Ruchika
    Oberg, Ann L.
    Zhang, Sheng
    Kohli, Manish
    [J]. CANCERS, 2020, 12 (09) : 1 - 24