PubMed:16033090 JSONTXT 8 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 0-189 DRI_Background denotes Expression of Her2/neu, steroid receptors (ER and PR), Ki67 and p53 in invasive mammary ductal carcinoma associated with ductal carcinoma In Situ (DCIS) Versus invasive breast cancer alone.
T2 196-487 DRI_Approach denotes (a) To assess the expression patterns of HER2/neu, steroid receptors (ER and PR), Ki67 and p53 in invasive ductal cancer (IDC) and IDC associated with carcinoma in situ (IDC/DCIS) and (b) to determine if there is a differential expression of these molecular markers between IDC and IDC/DCIS.
T3 511-678 DRI_Background denotes Paraffin-fixed breast cancer samples, diagnosed with only one histological invasive tumor (IDC (n=130), and IDC/DCIS (n=36) were analyzed by immunohistochemical means.
T4 679-801 DRI_Approach denotes The non-parametric Mann-Whitney and chi2 tests were used to evaluate any statistical differences between different groups.
T5 802-837 DRI_Unspecified denotes Significance was assumed at p<0.05.
T6 847-938 DRI_Unspecified denotes A significant increase of the tumor grading was observed between IDC and IDC/DCIS (p<0.05).
T7 939-1032 DRI_Unspecified denotes Her2/neu amplification was demonstrated in 49.6% of IDC compared to 31% of IDC/DCIS (p<0.05).
T8 1033-1106 DRI_Approach denotes ER expression showed no statistical differences between IDC and IDC/DCIS.
T9 1107-1214 DRI_Outcome denotes The PR expression was demonstrated in 71% of IDC with significantly lower intensity than IDC/DCIS (p<0.05).
T10 1215-1312 DRI_Outcome denotes The Ki67 expression was significantly higher (p<0.05) in IDC cases (64%) versus IDC/DCIS (49.7%).
T11 1313-1386 DRI_Approach denotes No differences were observed between IDC and IDC/DCIS for p53 expression.
T12 1399-1507 DRI_Outcome denotes We demonstrated significantly different expression patterns of Her2/neu, PR and Ki67 in IDC versus IDC/DCIS.
T13 1508-1673 DRI_Challenge denotes Since these molecular markers play important roles in carcinogenesis and tumor progression, IDC/DCIS could be an important subtype of mammary invasive ductal cancer.
T14 1674-1797 DRI_Challenge denotes Differences in expression of the evaluated markers might suggest a higher malignant potential of invasive carcinomas alone.
T15 1798-1927 DRI_Outcome denotes The lower expression of Her2/neu and Ki67 in IDC/DCIS could implicate a less malignant behavior compared to a differentiated IDC.
T16 1928-2105 DRI_Challenge denotes Additionally, these results might suggest that DCIS might be a malignant preform and the interaction with neoplastic tissue could result in an aggressive type of invasive tumor.