Paclitaxel-resistant human ovarian cancer cells have mutant β-tubulins that exhibit impaired paclitaxel-driven polymerization

Paraskevi Giannakakou, Dan L. Sackett, Yoon Koo Kang, Zhirong Zhan, Jeroen T.M. Buters, Tito Fojo, Marianne S. Poruchynsky

Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

671 Zitate (Scopus)

Abstract

Acquired resistance to paclitaxel can be mediated by P-glycoprotein or by alterations involving tubulin. We report two paclitaxel-resistant sublines derived from 1A9 human ovarian carcinoma cells. Single-step paclitaxel selection with verapamil yielded two clones that are resistant to paclitaxel and collaterally sensitive to vinblastine. The resistant sublines are not paclitaxel-dependent, and resistance remained stable after 3 years of drug- free culture. All cell lines accumulate [3H]paclitaxel equally, and no MDR- 1 mRNA was detected by polymerase chain reaction following reverse transcription. Total tubulin content is similar, but the polymerized fraction increased in parental but not in resistant cells following the paclitaxel addition. Purified tubulin from parental cells demonstrated paclitaxel- driven increased polymerization, in contrast to resistant cell tubulin, which did not polymerize under identical conditions. In contrast, epothilone B, an agent to which the resistant cells retained sensitivity, increased assembly. Comparable expression of β-tubulin isotypes was found in parental and resistant cells, with predominant expression of the M40 and β2 isotypes. Sequence analysis demonstrated acquired mutations in the M40 isotype at nucleotide 810 (T → G; Phe270 → Val) in 1A9PTX10 cells and nucleotide 1092 (G → A; Ala364 → Thr) in 1A9PTX22 cells. These results identify residues β270 and β364 as important modulators of paclitaxel's interaction with tubulin.

OriginalspracheEnglisch
Seiten (von - bis)17118-17125
Seitenumfang8
FachzeitschriftJournal of Biological Chemistry
Jahrgang272
Ausgabenummer27
DOIs
PublikationsstatusVeröffentlicht - 4 Juli 1997
Extern publiziertJa

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