Evidence map›Paper›PMID 7805177›Full record

ArticleCancer chemotherapy and pharmacology1995

In vivo screening models of cisplatin-resistant human lung cancer cell lines using SCID mice.

Y Heike, M Takahashi, T Ohira, H Arioka, Y Funayama, K Nishio, H Ogasawara, N Saijo

Abstract read
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Article in Cancer chemotherapy and pharmacology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Trial
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Y HeikePharmacology Division, National Cancer Center Research Institute, Tokyo, Japan.
M Takahashi
T Ohira
H Arioka
Y Funayama
K Nishio
H Ogasawara
N Saijo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In vivo screening models of a cisplatin (CDDP)-resistant human small-cell lung cancer cell (SCLC) line, H69/CDDP, and a non-small-cell lung cancer cell (NSCLC) line, PC-14/CDDP, were evaluated. The transplantability of the tumor xenografts to SCID mice was more than 90%. Tumor xenografts of H69/CDDP and PC-14/CDDP showed CDDP resistance during in vivo treatment. The novel anticancer agent 254-S showed only a partial effect on the growth of H69/CDDP and PC-14/CDDP while ormaplatin showed no cross resistance to CDDP. The in vivo results correlated well with the results of the in vitro MTT assay. In this in vivo sensitivity test, H69/CDDP and PC-14/CDDP were more sensitive to ormaplatin than its parental cell lines. In vivo sensitivity testing using SCID mice bearing transplanted CDDP-resistant tumors was shown to be useful for evaluating the effects of new anti-cancer drugs, especially those that might overcome CDDP resistance.

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, Non-Small-Cell LungCarcinoma, Small CellCell DivisionCisplatinDrug ResistanceFemaleHumansLung NeoplasmsMiceMice, SCIDNeoplasm TransplantationOrganoplatinum CompoundsTumor Cells, CulturedAntineoplastic AgentsCisplatinnedaplatinOrganoplatinum Compoundsormaplatin

Identifiers

PMID7805177

What OpenQuestion holds

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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.