The epithelial-mesenchymal transition (EMT) and colorectal cancer progression

During embryonic development, epithelial cells must escape the structural constraints imposed by tissue architecture and adopt a phenotype more amenable to cell movement, a process known as the epithelial-mesenchymal transition (EMT). The progression of carcinomas to invasive and metastatic disease...

Full description

Saved in:
Bibliographic Details
Published in:Cancer biology & therapy Vol. 4; no. 4; pp. 365 - 370
Main Authors: Bates, Richard C, Mercurio, Arthur M
Format: Journal Article
Language:English
Published: United States 01-04-2005
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract During embryonic development, epithelial cells must escape the structural constraints imposed by tissue architecture and adopt a phenotype more amenable to cell movement, a process known as the epithelial-mesenchymal transition (EMT). The progression of carcinomas to invasive and metastatic disease may also involve localized occurrences of EMT. However, data that support the actual occurrence of EMT in specific carcinomas and the relevance of this process to the progression of these tumors had been scant. This review highlights recent studies that substantiate the importance of the EMT to colorectal carcinoma. Specifically, a novel model for studying the EMT of colorectal carcinoma has been used to gain insight into the nature of the EMT itself and to identify molecular events that contribute to disease progression. Although loss of E-cadherin function is a primal event for the EMT, the expression of specific integrins such as alpha(v)beta6 as a consequence of the EMT enables invasive cells to interact with interstitial matrices and to sustain activation of TGF-beta. Of note, alpha(v)beta6 expression in tumors is a marker of cells that have undergone an EMT and it is prognostic for tumors that will progress more rapidly to terminal disease. The EMT also induces autocrine signaling involving VEGF and Flt-1 that enable invasive cells to become 'self-sufficient' for survival. Thus, the EMT appears to be an integral component of colorectal cancer progression and its analysis can yield novel targets for prognosis and therapy.
AbstractList During embryonic development, epithelial cells must escape the structural constraints imposed by tissue architecture and adopt a phenotype more amenable to cell movement, a process known as the epithelial-mesenchymal transition (EMT). The progression of carcinomas to invasive and metastatic disease may also involve localized occurrences of EMT. However, data that support the actual occurrence of EMT in specific carcinomas and the relevance of this process to the progression of these tumors had been scant. This review highlights recent studies that substantiate the importance of the EMT to colorectal carcinoma. Specifically, a novel model for studying the EMT of colorectal carcinoma has been used to gain insight into the nature of the EMT itself and to identify molecular events that contribute to disease progression. Although loss of E-cadherin function is a primal event for the EMT, the expression of specific integrins such as alpha(v)beta6 as a consequence of the EMT enables invasive cells to interact with interstitial matrices and to sustain activation of TGF-beta. Of note, alpha(v)beta6 expression in tumors is a marker of cells that have undergone an EMT and it is prognostic for tumors that will progress more rapidly to terminal disease. The EMT also induces autocrine signaling involving VEGF and Flt-1 that enable invasive cells to become 'self-sufficient' for survival. Thus, the EMT appears to be an integral component of colorectal cancer progression and its analysis can yield novel targets for prognosis and therapy.
Author Mercurio, Arthur M
Bates, Richard C
Author_xml – sequence: 1
  givenname: Richard C
  surname: Bates
  fullname: Bates, Richard C
  email: richard.bates@umassmed.edu
  organization: Division of Cancer Biology and Angiogenesis, Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachussetts, USA. richard.bates@umassmed.edu
– sequence: 2
  givenname: Arthur M
  surname: Mercurio
  fullname: Mercurio, Arthur M
BackLink https://www.ncbi.nlm.nih.gov/pubmed/15846061$$D View this record in MEDLINE/PubMed
BookMark eNo1kDtrwzAYRTWkNI_2LxRNpR0MkmU9PJaQPiChizsbWfpcu8iSK9lD_n0NTaY73MO5cLdo5YOHFdpQzlRWkEKu0TalH0JymYvyFq0pV4Uggm7QqeoAw9hPHbheu2yABN5050E7PEXtUz_1weOnw6l6xtpbbIILEcy09EZ7AxGPMXxHSGnh7tBNq12C-0vu0Nfrodq_Z8fPt4_9yzEbc1JOmeKqEaIlVFJmSaNsqYQlraES2oZJqXmpjSAs5xps0xJrrKW2EIpaqqnK2Q49_nuX7d8Z0lQPfTLgnPYQ5lQLVXDCaLGADxdwbgaw9Rj7QcdzfT2A_QHQDliH
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
7X8
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE
Database_xml – sequence: 1
  dbid: ECM
  name: MEDLINE
  url: https://search.ebscohost.com/login.aspx?direct=true&db=cmedm&site=ehost-live
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EndPage 370
ExternalDocumentID 15846061
Genre Journal Article
Review
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: NCI NIH HHS
  grantid: CA107548
– fundername: NIDDK NIH HHS
  grantid: DK34854
– fundername: NCI NIH HHS
  grantid: CA80789
GroupedDBID ---
00X
0VX
0YH
29B
30N
4.4
53G
5GY
6J9
ABCCY
ABEIZ
ABFIM
ACENM
ACGFO
ACGFS
ACKZS
ACTIO
ADBBV
ADCVX
ADFZZ
AECIN
AEGYZ
AEISY
AENEX
AEXWM
AFPKN
AGYJP
AIJEM
ALMA_UNASSIGNED_HOLDINGS
ALQZU
AOIJS
AQRUH
AURDB
AVBZW
BABNJ
BAWUL
BFWEY
BLEHA
C1A
CCCUG
CGR
CUY
CVF
CWRZV
DGEBU
DIK
DKSSO
E3Z
EBS
ECM
EIF
EJD
EMOBN
F5P
GROUPED_DOAJ
H13
HYE
IH2
IPNFZ
KSSTO
KYCEM
LJTGL
M4Z
NPM
O9-
OK1
P2P
P6G
PCLFJ
RIG
RPM
SJN
TDBHL
TFL
TFT
TFW
TR2
TTHFI
UDS
7X8
ID FETCH-LOGICAL-p209t-858b66f01713d0b8d986d0fc17efb377a59ac60325aedbf0dcdd1d4681d1a1823
ISSN 1538-4047
IngestDate Fri Oct 25 01:12:51 EDT 2024
Sat Sep 28 08:38:38 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 4
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-p209t-858b66f01713d0b8d986d0fc17efb377a59ac60325aedbf0dcdd1d4681d1a1823
Notes ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
PMID 15846061
PQID 68450314
PQPubID 23479
PageCount 6
ParticipantIDs proquest_miscellaneous_68450314
pubmed_primary_15846061
PublicationCentury 2000
PublicationDate 2005-Apr
20050401
PublicationDateYYYYMMDD 2005-04-01
PublicationDate_xml – month: 04
  year: 2005
  text: 2005-Apr
PublicationDecade 2000
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Cancer biology & therapy
PublicationTitleAlternate Cancer Biol Ther
PublicationYear 2005
SSID ssj0027269
Score 2.3096366
SecondaryResourceType review_article
Snippet During embryonic development, epithelial cells must escape the structural constraints imposed by tissue architecture and adopt a phenotype more amenable to...
SourceID proquest
pubmed
SourceType Aggregation Database
Index Database
StartPage 365
SubjectTerms Animals
Antigens, Neoplasm - metabolism
Biomarkers, Tumor
Colorectal Neoplasms - metabolism
Colorectal Neoplasms - pathology
Disease Progression
Epithelium - metabolism
Epithelium - pathology
Humans
Integrins - metabolism
Mesoderm - metabolism
Mesoderm - pathology
Transforming Growth Factor beta - metabolism
Tumor Necrosis Factor-alpha - metabolism
Vascular Endothelial Growth Factor A - metabolism
Title The epithelial-mesenchymal transition (EMT) and colorectal cancer progression
URI https://www.ncbi.nlm.nih.gov/pubmed/15846061
https://search.proquest.com/docview/68450314
Volume 4
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtZ3NS8MwFMCD8yBexO9vzcGDHgrtkrbJUWbHEDcPVvBW8lUm6Da67eB_70vTrR0o6sFLKCltoL_w8t7r-0DoKuQ5p3DyeyxX3AP9X3s8l7GnNVFKSRLJMhiz9xQPXthdQpO6FWQ996-kYQ5Y28zZP9BevhQm4BqYwwjUYfw1dzOxmRZvsJj3brOL1PDjvQwqh3PptQLOkn5qXQIurw2sdpB8tlaI3QWFC9tyJTua6mvH3V1UbrLbZrZalsB6RKeNjP3aC9s3hXXtu7SaYjacF5UnduFzCBuhKrWYpL6rlbmQo7SxXWhDJhLXDKI6XonrE7Ja-XrwmHWfHx6yNHlJW6hFAhuc-XQ_qE3ndtmccLnu9_ZAqRek22irUujxrSOxg9bMaBdt9KuQhT3UByD4ayC4BoKvAccNBhi4hoEdDNyAsY-eu0na6XlVDwtv0vb5zGMhk1GU26pERPuSac4i7ecqiE0uSRyLkAsV-aQdCqNl7muldaBpBGZEIMD2IwdofTQemSOEA2GU0AGToS8poULkHFQNGRl4hAdEHaPLxTfJQEbYHz9iZMbzaRYxGto2Bcfo0H2qbOJKmWSB1T9BpTv58dlTtFnvhDO0Pivm5hy1pnp-UaL6BNccPoU
link.rule.ids 315,782,786
linkProvider Multiple Vendors
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=The+epithelial-mesenchymal+transition+%28EMT%29+and+colorectal+cancer+progression&rft.jtitle=Cancer+biology+%26+therapy&rft.au=Bates%2C+Richard+C&rft.au=Mercurio%2C+Arthur+M&rft.date=2005-04-01&rft.issn=1538-4047&rft.volume=4&rft.issue=4&rft.spage=365&rft.epage=370&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1538-4047&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1538-4047&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1538-4047&client=summon