PubMed:9006344 JSONTXT 10 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T1 123-335 DRI_Background denotes Identical allelic loss in invasive and adjacent in situ ductal breast carcinoma (DCIS) on chromosome 11q13 has been previously reported, providing molecular evidence for the progression of DCIS to invasive tumor.
T2 336-554 DRI_Challenge denotes In this study we analyzed loss of heterozygosity (LOH) on 11q13 (PYGM, INT-2) in atypical ductal hyperplasia (ADH) and various histological types of in situ carcinomas of the breast in patients without invasive cancer.
T3 555-631 DRI_Background denotes Twenty-four cases of in situ carcinoma and twelve cases of ADH were studied.
T4 632-802 DRI_Background denotes Tissue microdissection of normal, hyperplastic, and tumor cells from fixed, paraffin-embedded sections was performed, and DNA was extracted for polymerase chain reaction.
T5 803-857 DRI_Background denotes In situ tumors included both high- and low-grade DCIS.
T6 858-957 DRI_Background denotes LOH was identified in six of twenty-two (27.3%) in situ tumors and in one of eleven (9%) ADH cases.
T7 958-1080 DRI_Background denotes Within in situ carcinomas, LOH was identified in six of seventeen (35%) high-grade DCIS but in none of six low-grade DCIS.
T8 1081-1278 DRI_Challenge denotes The present results show that LOH at 11q13 occurs in an appreciable proportion of high-grade DCIS, although the rate is substantially less than in patients with concomitant DCIS and invasive tumor.
T9 1279-1524 DRI_Background denotes LOH was identified less frequently in low-grade in situ tumors and ADH, suggesting that a putative tumor suppressor gene(s) located on chromosome 11q13 may be involved in the transition from early preneoplastic lesions to invasive breast cancer.