Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2010-7-16
pubmed:abstractText
Endometrial adenocarcinoma is the most common gynaecological malignancy in western countries. Many of the established risk factors for developing endometrial cancer are associated with excess exposure to oestrogen unopposed by progesterone. These include nulliparity, late onset of the menopause, post-menopausal hormone replacement therapy and obesity. However, a number of risk factors also promote inflammation, another feature proposed to influence cancer development. The human cycling endometrium undergoes regular and cyclical episodes of inflammation. Moreover, hormonal and genetic changes that occur early in the development of endometrial adenocarcinoma can exacerbate the local inflammatory environment. Via alterations in the expression of local mediators and immune cell function, these may contribute to the development of endometrial cancer. This review discusses the contribution of inflammation to the initiation and progression of endometrial adenocarcinoma. Manipulation of inflammatory pathways may therefore represent a therapeutic target in endometrial adenocarcinoma.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Androgens, http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, http://linkedlifedata.com/resource/pubmed/chemical/Cytokines, http://linkedlifedata.com/resource/pubmed/chemical/Estrogens, http://linkedlifedata.com/resource/pubmed/chemical/Glucocorticoids, http://linkedlifedata.com/resource/pubmed/chemical/KRAS protein, human, http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B, http://linkedlifedata.com/resource/pubmed/chemical/PTEN Phosphohydrolase, http://linkedlifedata.com/resource/pubmed/chemical/PTEN protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Progesterone, http://linkedlifedata.com/resource/pubmed/chemical/Prostaglandins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/ras Proteins
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1479-6805
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
206
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
141-57
pubmed:dateRevised
2010-10-4
pubmed:meshHeading
pubmed-meshheading:20406782-Adenocarcinoma, pubmed-meshheading:20406782-Androgens, pubmed-meshheading:20406782-Chemokines, pubmed-meshheading:20406782-Cytokines, pubmed-meshheading:20406782-Disease Progression, pubmed-meshheading:20406782-Endometrial Neoplasms, pubmed-meshheading:20406782-Estrogens, pubmed-meshheading:20406782-Female, pubmed-meshheading:20406782-Gene Expression Regulation, Neoplastic, pubmed-meshheading:20406782-Glucocorticoids, pubmed-meshheading:20406782-Humans, pubmed-meshheading:20406782-Inflammation, pubmed-meshheading:20406782-Leukocytes, pubmed-meshheading:20406782-Menstruation, pubmed-meshheading:20406782-Mutation, pubmed-meshheading:20406782-NF-kappa B, pubmed-meshheading:20406782-PTEN Phosphohydrolase, pubmed-meshheading:20406782-Progesterone, pubmed-meshheading:20406782-Prostaglandins, pubmed-meshheading:20406782-Proto-Oncogene Proteins, pubmed-meshheading:20406782-Risk Factors, pubmed-meshheading:20406782-Signal Transduction, pubmed-meshheading:20406782-Transcription, Genetic, pubmed-meshheading:20406782-Up-Regulation, pubmed-meshheading:20406782-ras Proteins
pubmed:year
2010
pubmed:articleTitle
Inflammatory events in endometrial adenocarcinoma.
pubmed:affiliation
MRC Human Reproductive Sciences Unit, The Queen's Medical Research Institute, Centre for Reproductive Biology, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't