2014
DOI: 10.4155/cli.14.62
|View full text |Cite
|
Sign up to set email alerts
|

HER2/neu: an increasingly important therapeutic target. Part 2: Distribution of HER2/neu overexpression and gene amplification by organ, tumor site and histology

Abstract: No biological molecule in the field of oncology has been more extensively or more successfully targeted for therapeutic intent than the product of the c-erbB2 gene, HER2/neu. This is the second of a comprehensive three-part review of the foundation for and therapeutic targeting of HER2/neu. The distribution of HER2/neu overexpression and/or gene amplification by individual tumor sites and histologies will be comprehensively surveyed and described. This provides a bridge between the primarily basic science focu… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
6
0
2

Year Published

2017
2017
2023
2023

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 12 publications
(9 citation statements)
references
References 385 publications
1
6
0
2
Order By: Relevance
“…Regarding chondrosarcoma, the level of immunohistochemical expression of HER-2 was similar in all cases as we didn’t find membranous staining in any of the examined cases. Our findings were just identical to those reported by Nelson et al and Park et al, [ 17 ] [ 29 ] who couldn’t detect immunohistochemical staining of HER-2 in their chondrosarcoma cases. Therefore, it is unlikely that targeted therapy against HER-2 overexpression could be used effectively in the treatment of such miserable patients also experiencing well-known resistance to most chemotherapeutic regimens.…”
Section: Discussionsupporting
confidence: 92%
See 1 more Smart Citation
“…Regarding chondrosarcoma, the level of immunohistochemical expression of HER-2 was similar in all cases as we didn’t find membranous staining in any of the examined cases. Our findings were just identical to those reported by Nelson et al and Park et al, [ 17 ] [ 29 ] who couldn’t detect immunohistochemical staining of HER-2 in their chondrosarcoma cases. Therefore, it is unlikely that targeted therapy against HER-2 overexpression could be used effectively in the treatment of such miserable patients also experiencing well-known resistance to most chemotherapeutic regimens.…”
Section: Discussionsupporting
confidence: 92%
“…The HER-2 expression has been recognised in some tumour types mainly breast, gastric, oesophageal, pancreatic, and many others. Even though there are agreement about antibodies and tyrosine kinase inhibitors targeting HER-2 in the breast, gastric and oesophagal adenocarcinomas, still there are other evident prospects in other tumour types [ 17 ].…”
Section: Discussionmentioning
confidence: 99%
“…HER2 is found to be over expressed in several breast cancers and correlates with tumor size and estrogen expression. Additionally, HER2 expression was reported to be amplified in 20–25% of breast cancers and acted as an indicator of poor prognosis [ 37 ]. On the other hand, mutations, aberrant or deregulated expression of TP53 , MDM2 and RB genes have also been implicated to play a key role in therapeutic responses to breast cancer [ 38 ].…”
Section: Breast Cancermentioning
confidence: 99%
“…Overactivity and overexpression of these proteins have also been implicated in the formation of malignancies of the Skin, Genitourinary tract, gastrointestinal tract, Head and Neck and Prostate. Our grasp of their complex function and molecular regulatory networks has fuelled the development of revolutionary therapeutic options in the management of cancers over the last decade [4].…”
Section: Introductionmentioning
confidence: 99%
“…The HER2/neu protein has been demonstrated to be an effective target in molecular therapy of metastatic cancers of the breast and stomach, via the use of monoclonal antibodies [e.g. Transtuzumab] specific for the Her-2/neu protein [4] [5]. Similarly, the use of monoclonal antibodies such as Cetuximab and the tyrosine kinase inhibitors, Gefitinib and Erlotinib, targeting EGFR has been rewarding in the treatment of non-small cell lung cancer, as well as cancers of the colon, pancreas and the prostate [6].…”
Section: Introductionmentioning
confidence: 99%