Mining metastasis related genes by primary-secondary tumor comparisons from large-scale databases

Cited 2 time in webofscience Cited 0 time in scopus
  • Hit : 537
  • Download : 379
Background: Metastasis is the most dangerous step in cancer progression and causes more than 90% of cancer death. Although many researchers have been working on biological features and characteristics of metastasis, most of its genetic level processes remain uncertain. Some studies succeeded in elucidating metastasis related genes and pathways, followed by predicting prognosis of cancer patients, but there still is a question whether the result genes or pathways contain enough information and noise features have been controlled appropriately. Methods: We set four tumor type classes composed of various tumor characteristics such as tissue origin, cellular environment, and metastatic ability. We conducted a set of comparisons among the four tumor classes followed by searching for genes that are consistently up or down regulated through the whole comparisons. Results: We identified four sets of genes that are consistently differently expressed in the comparisons, each of which denotes one of four cellular characteristics respectively - liver tissue, colon tissue, liver viability and metastasis characteristics. We found that our candidate genes for tissue specificity are consistent with the TiGER database. And we also found that the metastasis candidate genes from our method were more consistent with the known biological background and independent from other noise features. Conclusion: We suggested a new method for identifying metastasis related genes from a large-scale database. The proposed method attempts to minimize the influences from other factors except metastatic ability including tissue originality and tissue viability by confining the result of metastasis unrelated test combinations.
Publisher
BIOMED CENTRAL LTD
Issue Date
2009-03
Language
English
Article Type
Article
Keywords

PROSTATE-CANCER PROGRESSION; BREAST-CANCER; EXPRESSION; ACTIVATION; INVASION; RECEPTOR; PATHWAY; GENOME; BAP31

Citation

BMC BIOINFORMATICS, v.10

ISSN
1471-2105
URI
http://hdl.handle.net/10203/18463
Appears in Collection
BiS-Journal Papers(저널논문)
Files in This Item
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 2 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0