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PubMed:11489816 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 13-23 gene:9622 denotes kallikrein
T1 77-91 disease:C0029925 denotes ovarian cancer
T2 13-23 gene:9622 denotes kallikrein
T3 77-91 disease:C1140680 denotes ovarian cancer
R1 T0 T1 associated_with kallikrein,ovarian cancer
R2 T2 T3 associated_with kallikrein,ovarian cancer

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
11489816-0#13#23#gene9622 13-23 gene9622 denotes kallikrein
11489816-0#77#91#diseaseC0029925 77-91 diseaseC0029925 denotes ovarian cancer
11489816-0#77#91#diseaseC1140680 77-91 diseaseC1140680 denotes ovarian cancer
13#23#gene962277#91#diseaseC0029925 11489816-0#13#23#gene9622 11489816-0#77#91#diseaseC0029925 associated_with kallikrein,ovarian cancer
13#23#gene962277#91#diseaseC1140680 11489816-0#13#23#gene9622 11489816-0#77#91#diseaseC1140680 associated_with kallikrein,ovarian cancer

PubMed_Structured_Abstracts

Id Subject Object Predicate Lexical cue
T1 111-605 OBJECTIVE denotes Kallikrein gene 4 (KLK4, also known as prostase/KLK-L1), located on chromosome 19q13.4, is one of the newly discovered members of the human KLK-like gene family. This gene is up-regulated by androgens in the LNCaP prostatic carcinoma cell line and by androgens and progestins in the BT-474 breast cancer cell line. On the basis of its apparent association with hormonally regulated tissues, we have undertaken to examine the prognostic value of KLK4 expression in 147 malignant ovarian tissues.
T2 627-967 METHODS denotes Tumors were pulverized, total RNA was extracted, and cDNA was prepared by reverse transcription. KLK4 was amplified by PCR using gene-specific primers, and its identity was verified by sequencing. Ovarian tissues were then classified as KLK4-positive or -negative, based on ethidium bromide visualization of the PCR product on agarose gels.
T3 977-1602 RESULTS denotes KLK4 was found to be expressed in 69 (55%) of 147 of ovarian cancer samples. We found a strong positive association between KLK4 expression and tumor grade (P = 0.02) and clinical stage (P < 0.001). Univariate survival analysis revealed that patients with ovarian tumors positive for KLK4 expression had an increased risk for relapse and death (P = 0.003 and 0.001, respectively). Whereas knowledge of KLK4 status did not significantly increase the prognostic power of the multivariate models, additional analyses did determine that KLK4 was an independent unfavorable prognostic factor in patients with grade 1 and 2 tumors.
T4 1616-1718 CONCLUSIONS denotes Our findings indicate that KLK4 expression is associated with more aggressive forms of ovarian cancer.