Beta class II tubulin predominates in normal and tumor breast tissues.
Beta class II tubulin predominates in normal and tumor breast tissues.
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DOI:
10.1186/bcr631
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发表时间:
2003
期刊:
影响因子:
--
通讯作者:
Lobert S
中科院分区:
文献类型:
--
作者:
Dozier JH;Hiser L;Davis JA;Thomas NS;Tucci MA;Benghuzzi HA;Frankfurter A;Correia JJ;Lobert S
Antimitotic chemotherapeutic agents target tubulin, the major protein in mitotic spindles. Tubulin isotype composition is thought to be both diagnostic of tumor progression and a determinant of the cellular response to chemotherapy. This implies that there is a difference in isotype composition between normal and tumor tissues. To determine whether such a difference occurs in breast tissues, total tubulin was fractionated from lysates of paired normal and tumor breast tissues, and the amounts of β-tubulin classes I + IV, II, and III were measured by competitive enzyme-linked immunosorbent assay (ELISA). Only primary tumor tissues, before chemotherapy, were examined. Her2/neu protein amplification occurs in about 30% of breast tumors and is considered a marker for poor prognosis. To gain insight into whether tubulin isotype levels might be correlated with prognosis, ELISAs were used to quantify Her2/neu protein levels in these tissues. β-Tubulin isotype distributions in normal and tumor breast tissues were similar. The most abundant β-tubulin isotypes in these tissues were β-tubulin classes II and I + IV. Her2/neu levels in tumor tissues were 5–30-fold those in normal tissues, although there was no correlation between the Her2/neu biomarker and tubulin isotype levels. These results suggest that tubulin isotype levels, alone or in combination with Her2/neu protein levels, might not be diagnostic of tumorigenesis in breast cancer. However, the presence of a broad distribution of these tubulin isotypes (for example, 40–75% β-tubulin class II) in breast tissue, in conjunction with other factors, might still be relevant to disease progression and cellular response to antimitotic drugs.
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DOI:
10.1073/pnas.85.12.4530
发表时间:
1988-06-01
影响因子:
11.1
作者:
HOFFMAN, PN;CLEVELAND, DW
通讯作者:
CLEVELAND, DW
影响因子:
--
作者:
GONZALEZGARAY, ML;CABRAL, F
通讯作者:
CABRAL, F
影响因子:
2.9
作者:
Derry, WB;Wilson, L;Jordan, MA
通讯作者:
Jordan, MA
影响因子:
7.5
作者:
Cassimeris, L
通讯作者:
Cassimeris, L
影响因子:
3.3
作者:
DHAMODHARAN, R;JORDAN, MA;WADSWORTH, P
通讯作者:
WADSWORTH, P