Evolutionary Expression of HER2 Conferred by Chromosome Aneuploidy on Circulating Gastric Cancer Cells Contributes to Developing Targeted and Chemotherapeutic Resistance

Purpose: Previous human epidermal growth factor receptor-2 (HER2)-derived resistance studies were based on ex vivo models, which could not mirror evolutionary expression of HER2 during therapy. To investigate dynamic expression of HER2 and its contribution to developing therapeutic resistance confer...

Full description

Saved in:
Bibliographic Details
Published inClinical cancer research Vol. 24; no. 21; pp. 5261 - 5271
Main Authors Li, Yilin, Zhang, Xiaotian, Liu, Dan, Gong, Jifang, Wang, Daisy Dandan, Li, Shan, Peng, Zhi, Li, Yanyan, Wang, Xiaojuan, Lin, Peter Ping, Li, Min, Shen, Lin
Format Journal Article
LanguageEnglish
Published United States 01.11.2018
Online AccessGet full text

Cover

Loading…
Abstract Purpose: Previous human epidermal growth factor receptor-2 (HER2)-derived resistance studies were based on ex vivo models, which could not mirror evolutionary expression of HER2 during therapy. To investigate dynamic expression of HER2 and its contribution to developing therapeutic resistance conferred by chromosome aneuploidy, both the HER2 phenotype and chromosome 8 (Chr 8) aneuploidy on circulating tumor cells (CTC) were coexamined in advanced gastric cancer (AGC) patients. Experimental Design: A total of 115 AGC patients, including 56 of histopathologic HER2+ (hHER2+) subjects who received first-line HER2-targeted therapy plus chemotherapy, and 59 of hHER2− patients who received chemotherapy alone, were prospectively enrolled. Both HER2 phenotype and Chr8 aneuploidy of CTCs in patients were coexamined by HER2-iFISH during therapy. Results: A fluctuated positive HER2 phenotype on CTCs (cHER2+) was revealed, showing cHER2+ at different time intervals during treatment. Acquisition of the cHER2+ phenotype in 91.0% of hHER2+ and 76.2% hHER2− patients was demonstrated to correlate with development of resistance to trastuzumab-targeted therapy for hHER2+ patients and chemotherapy alone for hHER2− patients. Aneuploid Chr8 was demonstrated to participate in the acquisition of the cHER2+ phenotype, which provides a growth advantage to HER2+ CTCs against therapeutic pressure, leading to the development of therapeutic resistance. Conclusions: Compared with low positivity of conventional histopathologic hHER2 examination routinely performed once, significant higher positivity of cHER2+ on CTCs was observed. Continuously examining cHER2 shows unique advantages with respect to monitoring therapeutic resistance in real time in carcinoma patients. Moreover, contribution of chromosome aneuploidy to the phenotypic evolution of HER2 expression on CTCs may help elucidate underlying mechanisms of developing therapeutic resistance. Clin Cancer Res; 24(21); 5261–71. ©2018 AACR.
AbstractList Purpose: Previous human epidermal growth factor receptor-2 (HER2)-derived resistance studies were based on ex vivo models, which could not mirror evolutionary expression of HER2 during therapy. To investigate dynamic expression of HER2 and its contribution to developing therapeutic resistance conferred by chromosome aneuploidy, both the HER2 phenotype and chromosome 8 (Chr 8) aneuploidy on circulating tumor cells (CTC) were coexamined in advanced gastric cancer (AGC) patients.Experimental Design: A total of 115 AGC patients, including 56 of histopathologic HER2+ (hHER2+) subjects who received first-line HER2-targeted therapy plus chemotherapy, and 59 of hHER2- patients who received chemotherapy alone, were prospectively enrolled. Both HER2 phenotype and Chr8 aneuploidy of CTCs in patients were coexamined by HER2-iFISH during therapy.Results: A fluctuated positive HER2 phenotype on CTCs (cHER2+) was revealed, showing cHER2+ at different time intervals during treatment. Acquisition of the cHER2+ phenotype in 91.0% of hHER2+ and 76.2% hHER2- patients was demonstrated to correlate with development of resistance to trastuzumab-targeted therapy for hHER2+ patients and chemotherapy alone for hHER2- patients. Aneuploid Chr8 was demonstrated to participate in the acquisition of the cHER2+ phenotype, which provides a growth advantage to HER2+ CTCs against therapeutic pressure, leading to the development of therapeutic resistance.Conclusions: Compared with low positivity of conventional histopathologic hHER2 examination routinely performed once, significant higher positivity of cHER2+ on CTCs was observed. Continuously examining cHER2 shows unique advantages with respect to monitoring therapeutic resistance in real time in carcinoma patients. Moreover, contribution of chromosome aneuploidy to the phenotypic evolution of HER2 expression on CTCs may help elucidate underlying mechanisms of developing therapeutic resistance. Clin Cancer Res; 24(21); 5261-71. ©2018 AACR.Purpose: Previous human epidermal growth factor receptor-2 (HER2)-derived resistance studies were based on ex vivo models, which could not mirror evolutionary expression of HER2 during therapy. To investigate dynamic expression of HER2 and its contribution to developing therapeutic resistance conferred by chromosome aneuploidy, both the HER2 phenotype and chromosome 8 (Chr 8) aneuploidy on circulating tumor cells (CTC) were coexamined in advanced gastric cancer (AGC) patients.Experimental Design: A total of 115 AGC patients, including 56 of histopathologic HER2+ (hHER2+) subjects who received first-line HER2-targeted therapy plus chemotherapy, and 59 of hHER2- patients who received chemotherapy alone, were prospectively enrolled. Both HER2 phenotype and Chr8 aneuploidy of CTCs in patients were coexamined by HER2-iFISH during therapy.Results: A fluctuated positive HER2 phenotype on CTCs (cHER2+) was revealed, showing cHER2+ at different time intervals during treatment. Acquisition of the cHER2+ phenotype in 91.0% of hHER2+ and 76.2% hHER2- patients was demonstrated to correlate with development of resistance to trastuzumab-targeted therapy for hHER2+ patients and chemotherapy alone for hHER2- patients. Aneuploid Chr8 was demonstrated to participate in the acquisition of the cHER2+ phenotype, which provides a growth advantage to HER2+ CTCs against therapeutic pressure, leading to the development of therapeutic resistance.Conclusions: Compared with low positivity of conventional histopathologic hHER2 examination routinely performed once, significant higher positivity of cHER2+ on CTCs was observed. Continuously examining cHER2 shows unique advantages with respect to monitoring therapeutic resistance in real time in carcinoma patients. Moreover, contribution of chromosome aneuploidy to the phenotypic evolution of HER2 expression on CTCs may help elucidate underlying mechanisms of developing therapeutic resistance. Clin Cancer Res; 24(21); 5261-71. ©2018 AACR.
Purpose: Previous human epidermal growth factor receptor-2 (HER2)-derived resistance studies were based on ex vivo models, which could not mirror evolutionary expression of HER2 during therapy. To investigate dynamic expression of HER2 and its contribution to developing therapeutic resistance conferred by chromosome aneuploidy, both the HER2 phenotype and chromosome 8 (Chr 8) aneuploidy on circulating tumor cells (CTC) were coexamined in advanced gastric cancer (AGC) patients. Experimental Design: A total of 115 AGC patients, including 56 of histopathologic HER2+ (hHER2+) subjects who received first-line HER2-targeted therapy plus chemotherapy, and 59 of hHER2− patients who received chemotherapy alone, were prospectively enrolled. Both HER2 phenotype and Chr8 aneuploidy of CTCs in patients were coexamined by HER2-iFISH during therapy. Results: A fluctuated positive HER2 phenotype on CTCs (cHER2+) was revealed, showing cHER2+ at different time intervals during treatment. Acquisition of the cHER2+ phenotype in 91.0% of hHER2+ and 76.2% hHER2− patients was demonstrated to correlate with development of resistance to trastuzumab-targeted therapy for hHER2+ patients and chemotherapy alone for hHER2− patients. Aneuploid Chr8 was demonstrated to participate in the acquisition of the cHER2+ phenotype, which provides a growth advantage to HER2+ CTCs against therapeutic pressure, leading to the development of therapeutic resistance. Conclusions: Compared with low positivity of conventional histopathologic hHER2 examination routinely performed once, significant higher positivity of cHER2+ on CTCs was observed. Continuously examining cHER2 shows unique advantages with respect to monitoring therapeutic resistance in real time in carcinoma patients. Moreover, contribution of chromosome aneuploidy to the phenotypic evolution of HER2 expression on CTCs may help elucidate underlying mechanisms of developing therapeutic resistance. Clin Cancer Res; 24(21); 5261–71. ©2018 AACR.
Previous human epidermal growth factor receptor-2 (HER2)-derived resistance studies were based on models, which could not mirror evolutionary expression of HER2 during therapy. To investigate dynamic expression of HER2 and its contribution to developing therapeutic resistance conferred by chromosome aneuploidy, both HER2 phenotype and chromosome 8 aneuploidy on CTCs were co-examined in advanced gastric cancer (AGC) patients. Total of 115 AGC patients, including 56 of histo-pathological HER2 (hHER2 ) subjects who received first-line HER2-targeted therapy plus chemotherapy, and 59 of hHER2 patients who received chemotherapy alone, were prospectively enrolled. Both HER2 phenotype and Chr8 aneuploidy of CTCs in patients were co-examined by HER2-iFISH during therapy. A fluctuated positive HER2 phenotype on CTCs (cHER2 ) was revealed, showing cHER2 at different time intervals during treatment. Acquisition of cHER2 phenotype in 91.0% of hHER2 and 76.2% hHER2 patients was demonstrated to correlate with development of resistance to trastuzumab-targeted therapy for hHER2 patients and chemotherapy alone for hHER2 patients. Aneuploid Chr8 was demonstrated to participate in acquisition of cHER2 phenotype, which provides a growth advantage to HER2 CTCs against therapeutic pressure, leading to development of therapeutic resistance. Comparing to low positivity of conventional histo-pathological hHER2 examination routinely performed once, significant higher positivity of cHER2 on CTCs was observed. Continuously examining cHER2 possesses unique advantages with respect to monitoring therapeutic resistance in real time in carcinoma patients. Moreover, contribution of chromosome aneuploidy to phenotypic evolution of HER2 expression on CTCs may help elucidate underlying mechanisms of developing therapeutic resistance.
Author Li, Yilin
Wang, Daisy Dandan
Lin, Peter Ping
Li, Min
Li, Shan
Li, Yanyan
Zhang, Xiaotian
Gong, Jifang
Wang, Xiaojuan
Peng, Zhi
Liu, Dan
Shen, Lin
Author_xml – sequence: 1
  givenname: Yilin
  surname: Li
  fullname: Li, Yilin
– sequence: 2
  givenname: Xiaotian
  surname: Zhang
  fullname: Zhang, Xiaotian
– sequence: 3
  givenname: Dan
  surname: Liu
  fullname: Liu, Dan
– sequence: 4
  givenname: Jifang
  surname: Gong
  fullname: Gong, Jifang
– sequence: 5
  givenname: Daisy Dandan
  surname: Wang
  fullname: Wang, Daisy Dandan
– sequence: 6
  givenname: Shan
  surname: Li
  fullname: Li, Shan
– sequence: 7
  givenname: Zhi
  surname: Peng
  fullname: Peng, Zhi
– sequence: 8
  givenname: Yanyan
  surname: Li
  fullname: Li, Yanyan
– sequence: 9
  givenname: Xiaojuan
  surname: Wang
  fullname: Wang, Xiaojuan
– sequence: 10
  givenname: Peter Ping
  surname: Lin
  fullname: Lin, Peter Ping
– sequence: 11
  givenname: Min
  surname: Li
  fullname: Li, Min
– sequence: 12
  givenname: Lin
  surname: Shen
  fullname: Shen, Lin
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30012565$$D View this record in MEDLINE/PubMed
BookMark eNp9kctu1TAQhi1URC_wCCAv2aT4EjupWFXm0CJVQjoqa8uxJ61RYgfbqTiPxFviqD0bFqw8Hn3zz-U_RychBkDoPSWXlIr-EyVd35CWs0ul9g3tG8qIeIXOqBBdw5kUJzU-MqfoPOefhNCWkvYNOuU1ZEKKM_Rn9xSntfgYTDrg3e8lQc71h-OIb3d7hlUMI6QEDg8HrB5TnGOOM-DrAOsyRe8OuNLKJ7tOpvjwgG9MLslbrEywkLCCacqbTE0Oa4GMS8Rf4AmmuGz4vUkPUKq-Ca42gDmWR0hmgTqVxXvIPpdN6S16PZopw7uX9wL9-Lq7V7fN3febb-r6rrG8E6WpG1LhCLfOMc6pbAdhO8H5lbPUcN72bW-klS1lHQysG9hIGGupHB3rpQTJL9DHZ90lxV8r5KJnn21dwgSIa9aMdFRISfhVRT-8oOswg9NL8nM9oz6etwKfnwGbYs4JRm19Mdu1SzJ-0pTozUy9GaU3o3Q1U9OaqGbWavFP9bHB_-v-AqMEpII
CitedBy_id crossref_primary_10_3389_fbioe_2022_1015295
crossref_primary_10_3389_fonc_2022_821454
crossref_primary_10_1007_s00432_019_03040_9
crossref_primary_10_1002_cam4_3616
crossref_primary_10_1007_s10120_024_01486_6
crossref_primary_10_1002_1878_0261_13092
crossref_primary_10_3390_biom13010092
crossref_primary_10_1186_s12885_023_10985_1
crossref_primary_10_3389_fonc_2021_590952
crossref_primary_10_5230_jgc_2024_24_e5
crossref_primary_10_1007_s10238_023_01158_2
crossref_primary_10_1007_s10549_020_05662_x
crossref_primary_10_1002_ctm2_128
crossref_primary_10_1007_s13577_021_00568_2
crossref_primary_10_1016_j_canlet_2019_10_041
crossref_primary_10_3390_ijms24076791
crossref_primary_10_1016_j_semcancer_2019_08_026
crossref_primary_10_3390_cells9061539
crossref_primary_10_3389_fonc_2022_981907
crossref_primary_10_1111_1759_7714_14120
crossref_primary_10_1515_medgen_2023_2056
crossref_primary_10_1007_s00280_021_04251_z
crossref_primary_10_3390_cancers13205108
crossref_primary_10_1007_s10549_023_06942_y
crossref_primary_10_52927_jdcr_2024_12_2_106
crossref_primary_10_3389_fmed_2021_749250
crossref_primary_10_1002_adtp_202300044
crossref_primary_10_1186_s40364_020_00240_1
crossref_primary_10_1016_j_canlet_2023_216337
crossref_primary_10_1111_cas_15516
crossref_primary_10_1007_s10238_024_01310_6
crossref_primary_10_1007_s13577_023_00990_8
crossref_primary_10_1016_j_canlet_2024_217099
crossref_primary_10_3390_cancers12030695
crossref_primary_10_3892_ol_2024_14285
crossref_primary_10_1016_j_canlet_2021_06_002
crossref_primary_10_1016_S0140_6736_20_31288_5
crossref_primary_10_1177_17588359231183678
crossref_primary_10_3389_fonc_2022_828368
Cites_doi 10.1158/1535-7163.MCT-11-0754
10.1038/msb.2012.40
10.1016/j.ejca.2015.09.018
10.1186/2193-1801-2-386
10.1016/j.cell.2011.02.013
10.1200/JCO.2014.56.6851
10.1016/S1470-2045(13)70436-4
10.1016/S1470-2045(17)30111-0
10.3390/diagnostics8020026
10.1053/j.gastro.2016.05.052
10.1186/s13059-017-1328-6
10.1016/j.ccr.2014.02.025
10.1158/2159-8290.CD-15-1483
10.1016/j.ccell.2017.01.002
10.1038/nrclinonc.2016.15
10.1016/j.ccell.2015.06.007
10.1038/nature19328
10.1038/nrc.2017.69
10.1002/ijc.30383
10.1002/ijc.30408
10.1038/s41598-017-10763-7
10.1126/science.1235122
10.7554/eLife.03023
10.1038/bjc.2015.417
10.18632/oncotarget.2175
10.1038/embor.2012.55
10.1038/ncomms10754
10.1016/j.canlet.2017.10.004
10.1200/JCO.2013.53.6136
10.18632/oncotarget.3712
10.1007/s00262-014-1541-z
10.1038/nature09529
10.1158/0008-5472.CAN-16-3052
10.1016/j.ejca.2008.10.026
10.3322/caac.21387
10.1126/science.aaf6546
10.1016/S0140-6736(16)30354-3
10.1158/2159-8290.CD-17-0343
10.18632/oncotarget.4819
10.1038/srep22828
10.1016/S0140-6736(10)61121-X
ContentType Journal Article
Copyright Copyright ©2018, American Association for Cancer Research.
2018 American Association for Cancer Research.
Copyright_xml – notice: Copyright ©2018, American Association for Cancer Research.
– notice: 2018 American Association for Cancer Research.
DBID AAYXX
CITATION
NPM
7X8
DOI 10.1158/1078-0432.CCR-18-1205
DatabaseName CrossRef
PubMed
MEDLINE - Academic
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
CrossRef
PubMed
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1557-3265
EndPage 5271
ExternalDocumentID 30012565
10_1158_1078_0432_CCR_18_1205
Genre Journal Article
GroupedDBID ---
18M
29B
2FS
2WC
34G
39C
53G
5GY
5RE
5VS
6J9
AAFWJ
AAJMC
AAYXX
ABOCM
ACGFO
ACIWK
ACPRK
ACSVP
ADBBV
ADCOW
ADNWM
AENEX
AFHIN
AFOSN
AFRAH
AFUMD
ALMA_UNASSIGNED_HOLDINGS
BAWUL
BR6
BTFSW
CITATION
CS3
DIK
DU5
E3Z
EBS
EJD
F5P
FRP
GX1
H13
IH2
KQ8
L7B
LSO
OK1
P0W
P2P
QTD
RCR
RHI
RNS
SJN
TR2
W2D
W8F
WOQ
YKV
NPM
7X8
ID FETCH-LOGICAL-c375t-41015d03cdd233164b5c75339dc1a334848a6c64127eb27b2f022416fd2866e63
ISSN 1078-0432
1557-3265
IngestDate Fri Jul 11 06:38:15 EDT 2025
Thu Apr 03 07:00:44 EDT 2025
Thu Apr 24 22:57:43 EDT 2025
Tue Jul 01 01:30:16 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 21
Language English
License Copyright ©2018, American Association for Cancer Research.
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c375t-41015d03cdd233164b5c75339dc1a334848a6c64127eb27b2f022416fd2866e63
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0002-6869-9490
PMID 30012565
PQID 2071566039
PQPubID 23479
PageCount 11
ParticipantIDs proquest_miscellaneous_2071566039
pubmed_primary_30012565
crossref_citationtrail_10_1158_1078_0432_CCR_18_1205
crossref_primary_10_1158_1078_0432_CCR_18_1205
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2018-11-01
PublicationDateYYYYMMDD 2018-11-01
PublicationDate_xml – month: 11
  year: 2018
  text: 2018-11-01
  day: 01
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Clinical cancer research
PublicationTitleAlternate Clin Cancer Res
PublicationYear 2018
References Park (2022061107344649500_bib10) 2016; 53
Thuss-Patience (2022061107344649500_bib7) 2017; 18
Pietrantonio (2022061107344649500_bib14) 2016; 139
Eisenhauer (2022061107344649500_bib26) 2009; 45
Stingele (2022061107344649500_bib37) 2012; 8
Passerini (2022061107344649500_bib41) 2016; 7
Lin (2022061107344649500_bib29) 2018; 8
Chen (2022061107344649500_bib28) 2012; 11
Dephoure (2022061107344649500_bib36) 2014; 3
Domingues (2022061107344649500_bib38) 2017; 77
Bardelli (2022061107344649500_bib19) 2017; 31
Li (2022061107344649500_bib25) 2014; 5
Pavelka (2022061107344649500_bib35) 2010; 468
Siegel (2022061107344649500_bib3) 2017; 67
Hanahan (2022061107344649500_bib34) 2011; 144
Amirouchene-Angelozzi (2022061107344649500_bib12) 2017; 7
McGranahan (2022061107344649500_bib13) 2015; 28
Lordick (2022061107344649500_bib5) 2016; 13
Nagrath (2022061107344649500_bib15) 2016; 151
Zheng (2022061107344649500_bib27) 2014; 63
Maley (2022061107344649500_bib11) 2017; 17
Jordan (2022061107344649500_bib31) 2016; 537
Nishikawa (2022061107344649500_bib6) 2017; 140
Shen (2022061107344649500_bib1) 2013; 14
Liu (2022061107344649500_bib18) 2014; 32
Satoh (2022061107344649500_bib8) 2014; 32
Jiang (2022061107344649500_bib23) 2015; 6
Holland (2022061107344649500_bib40) 2012; 13
Van Cutsem (2022061107344649500_bib2) 2016; 388
Alix-Panabieres (2022061107344649500_bib17) 2016; 6
Wang (2022061107344649500_bib21) 2018; 412
Lin (2022061107344649500_bib22) 2017; 7
Bang (2022061107344649500_bib4) 2010; 376
Lin (2022061107344649500_bib32) 2017; 18
Ge (2022061107344649500_bib24) 2015; 6
Arteaga (2022061107344649500_bib9) 2014; 25
Cheung (2022061107344649500_bib20) 2016; 352
Luoh (2022061107344649500_bib30) 2013; 2
Rutledge (2022061107344649500_bib39) 2016; 6
Li (2022061107344649500_bib16) 2016; 114
Vogelstein (2022061107344649500_bib33) 2013; 339
References_xml – volume: 11
  start-page: 660
  year: 2012
  ident: 2022061107344649500_bib28
  article-title: MET activation mediates resistance to lapatinib inhibition of HER2-amplified gastric cancer cells
  publication-title: Mol Cancer Ther
  doi: 10.1158/1535-7163.MCT-11-0754
– volume: 8
  start-page: 608
  year: 2012
  ident: 2022061107344649500_bib37
  article-title: Global analysis of genome, transcriptome and proteome reveals the response to aneuploidy in human cells
  publication-title: Mol Syst Biol
  doi: 10.1038/msb.2012.40
– volume: 53
  start-page: 42
  year: 2016
  ident: 2022061107344649500_bib10
  article-title: Extra-gain of HER2-positive cases through HER2 reassessment in primary and metastatic sites in advanced gastric cancer with initially HER2-negative primary tumours: results of GASTric cancer HER2 reassessment study 1 (GASTHER1)
  publication-title: Eur J Cancer
  doi: 10.1016/j.ejca.2015.09.018
– volume: 2
  start-page: 386
  year: 2013
  ident: 2022061107344649500_bib30
  article-title: HER-2 gene amplification in human breast cancer without concurrent HER-2 over-expression
  publication-title: Springerplus
  doi: 10.1186/2193-1801-2-386
– volume: 144
  start-page: 646
  year: 2011
  ident: 2022061107344649500_bib34
  article-title: Hallmarks of cancer: the next generation
  publication-title: Cell
  doi: 10.1016/j.cell.2011.02.013
– volume: 32
  start-page: 3479
  year: 2014
  ident: 2022061107344649500_bib18
  article-title: By the numbers: does circulating tumor cell enumeration have a role in metastatic breast cancer?
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2014.56.6851
– volume: 14
  start-page: e535
  year: 2013
  ident: 2022061107344649500_bib1
  article-title: Management of gastric cancer in Asia: resource-stratified guidelines
  publication-title: Lancet Oncol
  doi: 10.1016/S1470-2045(13)70436-4
– volume: 18
  start-page: 640
  year: 2017
  ident: 2022061107344649500_bib7
  article-title: Trastuzumab emtansine versus taxane use for previously treated HER2-positive locally advanced or metastatic gastric or gastro-oesophageal junction adenocarcinoma (GATSBY): an international randomised, open-label, adaptive, phase 2/3 study
  publication-title: Lancet Oncol
  doi: 10.1016/S1470-2045(17)30111-0
– volume: 8
  start-page: 26
  year: 2018
  ident: 2022061107344649500_bib29
  article-title: Aneuploid CTC and CEC
  publication-title: Diagnostics
  doi: 10.3390/diagnostics8020026
– volume: 151
  start-page: 412
  year: 2016
  ident: 2022061107344649500_bib15
  article-title: Opportunities and challenges for pancreatic circulating tumor cells
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2016.05.052
– volume: 18
  start-page: 192
  year: 2017
  ident: 2022061107344649500_bib32
  article-title: Substantial contribution of genetic variation in the expression of transcription factors to phenotypic variation revealed by eRD-GWAS
  publication-title: Genome Biol
  doi: 10.1186/s13059-017-1328-6
– volume: 25
  start-page: 282
  year: 2014
  ident: 2022061107344649500_bib9
  article-title: ERBB receptors: from oncogene discovery to basic science to mechanism-based cancer therapeutics
  publication-title: Cancer Cell
  doi: 10.1016/j.ccr.2014.02.025
– volume: 6
  start-page: 479
  year: 2016
  ident: 2022061107344649500_bib17
  article-title: Clinical applications of circulating tumor cells and circulating tumor DNA as liquid biopsy
  publication-title: Cancer Discov
  doi: 10.1158/2159-8290.CD-15-1483
– volume: 31
  start-page: 172
  year: 2017
  ident: 2022061107344649500_bib19
  article-title: Liquid biopsies, what we do not know (yet)
  publication-title: Cancer Cell
  doi: 10.1016/j.ccell.2017.01.002
– volume: 13
  start-page: 348
  year: 2016
  ident: 2022061107344649500_bib5
  article-title: Clinical impact of tumour biology in the management of gastroesophageal cancer
  publication-title: Nat Rev Clin Oncol
  doi: 10.1038/nrclinonc.2016.15
– volume: 28
  start-page: 141
  year: 2015
  ident: 2022061107344649500_bib13
  article-title: Biological and therapeutic impact of intratumor heterogeneity in cancer evolution
  publication-title: Cancer Cell
  doi: 10.1016/j.ccell.2015.06.007
– volume: 537
  start-page: 102
  year: 2016
  ident: 2022061107344649500_bib31
  article-title: HER2 expression identifies dynamic functional states within circulating breast cancer cells
  publication-title: Nature
  doi: 10.1038/nature19328
– volume: 17
  start-page: 605
  year: 2017
  ident: 2022061107344649500_bib11
  article-title: Classifying the evolutionary and ecological features of neoplasms
  publication-title: Nat Rev Cancer
  doi: 10.1038/nrc.2017.69
– volume: 140
  start-page: 188
  year: 2017
  ident: 2022061107344649500_bib6
  article-title: Phase II study of the effectiveness and safety of trastuzumab and paclitaxel for taxane- and trastuzumab-naive patients with HER2-positive, previously treated, advanced, or recurrent gastric cancer (JFMC45-1102)
  publication-title: Int J Cancer
  doi: 10.1002/ijc.30383
– volume: 139
  start-page: 2859
  year: 2016
  ident: 2022061107344649500_bib14
  article-title: HER2 loss in HER2-positive gastric or gastroesophageal cancer after trastuzumab therapy: Implication for further clinical research
  publication-title: Int J Cancer
  doi: 10.1002/ijc.30408
– volume: 7
  start-page: 9789
  year: 2017
  ident: 2022061107344649500_bib22
  article-title: Comprehensive in situ co-detection of aneuploid circulating endothelial and tumor cells
  publication-title: Sci Rep
  doi: 10.1038/s41598-017-10763-7
– volume: 339
  start-page: 1546
  year: 2013
  ident: 2022061107344649500_bib33
  article-title: Cancer genome landscapes
  publication-title: Science
  doi: 10.1126/science.1235122
– volume: 3
  start-page: e03023
  year: 2014
  ident: 2022061107344649500_bib36
  article-title: Quantitative proteomic analysis reveals posttranslational responses to aneuploidy in yeast
  publication-title: Elife
  doi: 10.7554/eLife.03023
– volume: 114
  start-page: 138
  year: 2016
  ident: 2022061107344649500_bib16
  article-title: Dynamic monitoring of circulating tumour cells to evaluate therapeutic efficacy in advanced gastric cancer
  publication-title: Br J Cancer
  doi: 10.1038/bjc.2015.417
– volume: 5
  start-page: 6594
  year: 2014
  ident: 2022061107344649500_bib25
  article-title: Clinical significance of phenotyping and karyotyping of circulating tumor cells in patients with advanced gastric cancer
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.2175
– volume: 13
  start-page: 501
  year: 2012
  ident: 2022061107344649500_bib40
  article-title: Losing balance: the origin and impact of aneuploidy in cancer
  publication-title: Embo Reports
  doi: 10.1038/embor.2012.55
– volume: 7
  start-page: 10754
  year: 2016
  ident: 2022061107344649500_bib41
  article-title: The presence of extra chromosomes leads to genomic instability
  publication-title: Nat Commun
  doi: 10.1038/ncomms10754
– volume: 412
  start-page: 99
  year: 2018
  ident: 2022061107344649500_bib21
  article-title: Quantified postsurgical small cell size CTCs and EpCAM(+) circulating tumor stem cells with cytogenetic abnormalities in hepatocellular carcinoma patients determine cancer relapse
  publication-title: Cancer Lett
  doi: 10.1016/j.canlet.2017.10.004
– volume: 32
  start-page: 2039
  year: 2014
  ident: 2022061107344649500_bib8
  article-title: Lapatinib plus paclitaxel versus paclitaxel alone in the second-line treatment of HER2-amplified advanced gastric cancer in Asian populations: TyTAN–a randomized, phase III study
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2013.53.6136
– volume: 6
  start-page: 15639
  year: 2015
  ident: 2022061107344649500_bib23
  article-title: Comprehensive characterization of chemotherapeutic efficacy on metastases in the established gastric neuroendocrine cancer patient derived xenograft model
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.3712
– volume: 63
  start-page: 581
  year: 2014
  ident: 2022061107344649500_bib27
  article-title: Combining trastuzumab and cetuximab combats trastuzumab-resistant gastric cancer by effective inhibition of EGFR/ErbB2 heterodimerization and signaling
  publication-title: Cancer Immunol Immunother
  doi: 10.1007/s00262-014-1541-z
– volume: 468
  start-page: 321
  year: 2010
  ident: 2022061107344649500_bib35
  article-title: Aneuploidy confers quantitative proteome changes and phenotypic variation in budding yeast
  publication-title: Nature
  doi: 10.1038/nature09529
– volume: 77
  start-page: 2914
  year: 2017
  ident: 2022061107344649500_bib38
  article-title: Cellular prion protein PrP(C) and Ecto-5′-Nucleotidase are markers of the cellular stress response to aneuploidy
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-16-3052
– volume: 45
  start-page: 228
  year: 2009
  ident: 2022061107344649500_bib26
  article-title: New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1)
  publication-title: Eur J Cancer
  doi: 10.1016/j.ejca.2008.10.026
– volume: 67
  start-page: 7
  year: 2017
  ident: 2022061107344649500_bib3
  article-title: Cancer statistics, 2017
  publication-title: CA Cancer J Clin
  doi: 10.3322/caac.21387
– volume: 352
  start-page: 167
  year: 2016
  ident: 2022061107344649500_bib20
  article-title: A collective route to metastasis: Seeding by tumor cell clusters
  publication-title: Science
  doi: 10.1126/science.aaf6546
– volume: 388
  start-page: 2654
  year: 2016
  ident: 2022061107344649500_bib2
  article-title: Gastric cancer
  publication-title: Lancet
  doi: 10.1016/S0140-6736(16)30354-3
– volume: 7
  start-page: 805
  year: 2017
  ident: 2022061107344649500_bib12
  article-title: Tumor evolution as a therapeutic target
  publication-title: Cancer Discov
  doi: 10.1158/2159-8290.CD-17-0343
– volume: 6
  start-page: 27049
  year: 2015
  ident: 2022061107344649500_bib24
  article-title: Enhanced detection and comprehensive in situ phenotypic characterization of circulating and disseminated heteroploid epithelial and glioma tumor cells
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.4819
– volume: 6
  start-page: 22828
  year: 2016
  ident: 2022061107344649500_bib39
  article-title: Selective advantage of trisomic human cells cultured in non-standard conditions
  publication-title: Sci Rep
  doi: 10.1038/srep22828
– volume: 376
  start-page: 687
  year: 2010
  ident: 2022061107344649500_bib4
  article-title: Trastuzumab in combination with chemotherapy versus chemotherapy alone for treatment of HER2-positive advanced gastric or gastro-oesophageal junction cancer (ToGA): a phase 3, open-label, randomised controlled trial
  publication-title: Lancet
  doi: 10.1016/S0140-6736(10)61121-X
SSID ssj0014104
Score 2.483616
Snippet Purpose: Previous human epidermal growth factor receptor-2 (HER2)-derived resistance studies were based on ex vivo models, which could not mirror evolutionary...
Previous human epidermal growth factor receptor-2 (HER2)-derived resistance studies were based on models, which could not mirror evolutionary expression of...
SourceID proquest
pubmed
crossref
SourceType Aggregation Database
Index Database
Enrichment Source
StartPage 5261
Title Evolutionary Expression of HER2 Conferred by Chromosome Aneuploidy on Circulating Gastric Cancer Cells Contributes to Developing Targeted and Chemotherapeutic Resistance
URI https://www.ncbi.nlm.nih.gov/pubmed/30012565
https://www.proquest.com/docview/2071566039
Volume 24
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELZWRUJcEG-2PGQkbqssifPcI0oXLdByqLbScopiryNFSpNqm6CWf8Rv4s8wYztOKOVRLtHKSsZR5tvxjD3zDSGvOSvkImHCkeAMOQEX3Mm9RDoFLwRjqiMjFicffYpWJ8GHTbiZTL6Pspa6ls_F12vrSv5HqzAGesUq2Rto1gqFAfgN-oUraBiu_6Tj5RcjHlPflhcmp1U5gKvlMTPlfDvtZCIN7mlz3pwiE4nszqqmRDrpepaWO6GaeOFWVI59PMQsRTDsZqmsKtXUU_fF0nQQB0Od1VrlkUtF9zpD7oFxPRceDaB32sOq50PoazGFnsPQDdlt6UOVX_C5rEqLW7urvSnzph0B-rDsTJ28zSPqU4zLIjeLstnT8BJT3DeYYRd5fwOz8ymNaQ7BHDLdWaK33br-2mBUl1obSxwyTfJuVvWQ6U4vv64YYaI2L8yE8zQ9dvCFmBsOS2SfFnBl5bT5jCqSCpMMxWQoJgMxmQcDDPl1bzGIYbC9xsH7j_aIK_BUb0s7sykvAzFvrn2bnx2n30RDyita3yN3TThD32ps3icTWT8gt49MwsZD8m0MUTpAlDYFRYhSC1HKL-kAUTpAlMLdI4hSA1GqIUoVROkIorRt6ABR2kOUAkTpVYjSAaKPyMm75TpdOaY7iCP8OGwd-H5euHV9sd0y34eon4cCYm9_sRVejvXlQZJHIgo8FkvOYjBKyl2Nii1LokhG_mOyVze1fEqoV8Rgm1gRC8nBP-MLV-TgeEewtsmYe2JKgv7TZ8JQ52MHlyr7o-KnZG4fO9PcMX974FWv1wysPB7d5bVsuvOMQSQAgZfrL6bkiVa4FeljyAJx2f5Np3tG7gx_vudkr9118gW42C1_qaD6Awocz9U
linkProvider Flying Publisher
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Evolutionary+Expression+of+HER2+Conferred+by+Chromosome+Aneuploidy+on+Circulating+Gastric+Cancer+Cells+Contributes+to+Developing+Targeted+and+Chemotherapeutic+Resistance&rft.jtitle=Clinical+cancer+research&rft.au=Li%2C+Yilin&rft.au=Zhang%2C+Xiaotian&rft.au=Liu%2C+Dan&rft.au=Gong%2C+Jifang&rft.date=2018-11-01&rft.issn=1078-0432&rft.eissn=1557-3265&rft.volume=24&rft.issue=21&rft.spage=5261&rft.epage=5271&rft_id=info:doi/10.1158%2F1078-0432.CCR-18-1205&rft.externalDBID=n%2Fa&rft.externalDocID=10_1158_1078_0432_CCR_18_1205
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1078-0432&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1078-0432&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1078-0432&client=summon