Evidence map›Paper›PMID 20959065›Full record

ArticleZhongguo fei ai za zhi = Chinese journal of lung cancer2010

[Paclitaxel blocks immunologic escape through up-regulating TAP-1, TAP-2 and eliminatiing Treg cells in 3LL-bearing mice].

Hua Zhong, Baohui Han

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In one paragraph

Article in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed, 0 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Hua ZhongDepartment of Pulmonary Medicine, Shanghai Chest Hospital, Shanghai 200030, China.
Baohui Han
Shanghai Chest Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveUntil now, there are still some questions that chemotherapy could block cancer immunologic escape or not. The aim of this study is to explore the mechanism of paclitaxel in the blocking of immunologic escape in 3LL bearing mice.

methodsMHC class I components were detected by FACS antibodies TAP-1 and TAP-2 in 3LL group and 3LL pretreated with 5*10(-8) mmol/L paclitaxel. C57BL/6 mice were divided into 3 groups: tumor -bearing group, paclitaxel-treating group and tumor-free group. 3LL cells (0.3*10(6)) were injected via tail vein of mice. On day 8, paclitaxel (0.012 5 mg) was injected subcutaneously in the treatment group. On day 21, murine lung cells were suspended. With FACS triple staining, we analyzed expression of Treg in each group.

resultsThe expression of TAP-1 (5.68%+/-0.65%), TAP-2 (89.54%+/-4.8%) was remarkably higher in paclitaxel-pretreating 3LL group than that in 3LL bearing mice group with TAP-1 (1.93%+/-0.25%), TAP-2 (67.78%+/-5.08%), P=0.006, P=0.036 respectively. The expression of regulatory T cells (Treg) in tumor bearing mice was significantly higher (25.46%+/-2.23%) than that of in normal mice (12.46%+/-1.21%) (P < 0.001). Expression of Treg in paclitaxel treated mice was remarkably inhibited (17.53%+/-1.24%) compared with that in 3LL bearing mice group (P=0.004).

conclusionsPaclitaxel may block immunologic escape in the treatment of 3LL bearing mice partly through up-regulation TAP-1, TAP-2 and eliminating Treg cells.

Indexed as

AnimalsAntineoplastic AgentsATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily B, Member 2ATP Binding Cassette Transporter, Subfamily B, Member 3Cell Line, TumorFlow CytometryGene Expression Regulation, NeoplasticMaleMicePaclitaxelT-Lymphocytes, RegulatoryTumor EscapeUp-RegulationAntineoplastic AgentsATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily B, Member 2ATP Binding Cassette Transporter, Subfamily B, Member 3PaclitaxelTap1 protein, mouseTap2 protein, mouse

Identifiers

PMID20959065
PMCPMC6000582
OpenAlexW2287726312

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.