Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6C
pubmed:dateCreated
2008-1-24
pubmed:abstractText
Determining an effective predictor of clinical drug resistance in small cell lung cancer (SCLC) is considered to be important. In this study, the relationship between the expression of P-glycoprotein (P-gp), multidrug resistance-associated protein 1 (MRP1) and MRP2, which are the members of ATP-binding cassette superfamily transporter, and of the p53 tumor suppressor gene and the response to chemotherapy were analysed. The expression of P-gp, MRP1, MRP2, and p53 was determined by an immunohistochemical analysis of transbronchial biopsy (TBB) specimens from 61 SCLC patients. The relationship of such expression was also investigated regarding chemotherapy and clinicopathological factors. The response rate in the MRP2-negative group was significantly higher than that in the MRP2-positive group (88% versus 50%). The P-gp-negative group responded significantly better to chemotherapy than the P-gp-positive group, with a response rate of 81% versus 39%. No relationship could be found between the response to chemotherapy and immunostaining for MRP1 or p53. In 37 patients treated with platinum-based chemotherapy, the response rate of patients in the MRP2-negative group was significantly higher than that in the positive group (92% versus 50%). In a multiple logistic regression analysis, MRP2 as well as P-gp were shown to be statistically significant predictors of chemotherapy resistance. These results suggest that immunostaining of MRP2 for TBB specimens may help to predict clinical resistance to platinum agents. This is the first report which indicates that the immunohistochemical expression of MRP2 is positively related to a clinical resistance to platinum.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0250-7005
pubmed:author
pubmed:issnType
Print
pubmed:volume
27
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4351-8
pubmed:meshHeading
pubmed-meshheading:18214043-Adult, pubmed-meshheading:18214043-Aged, pubmed-meshheading:18214043-Aged, 80 and over, pubmed-meshheading:18214043-Antineoplastic Agents, pubmed-meshheading:18214043-Carcinoma, Small Cell, pubmed-meshheading:18214043-Drug Resistance, Multiple, pubmed-meshheading:18214043-Drug Resistance, Neoplasm, pubmed-meshheading:18214043-Female, pubmed-meshheading:18214043-Gene Expression, pubmed-meshheading:18214043-Humans, pubmed-meshheading:18214043-Immunohistochemistry, pubmed-meshheading:18214043-Lung Neoplasms, pubmed-meshheading:18214043-Male, pubmed-meshheading:18214043-Membrane Transport Proteins, pubmed-meshheading:18214043-Middle Aged, pubmed-meshheading:18214043-Multidrug Resistance-Associated Proteins, pubmed-meshheading:18214043-P-Glycoprotein, pubmed-meshheading:18214043-Platinum Compounds
pubmed:articleTitle
Immunohistochemical expression of MRP2 and clinical resistance to platinum-based chemotherapy in small cell lung cancer.
pubmed:affiliation
Research Institute for Diseases of the Chest, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
pubmed:publicationType
Journal Article