Evidence map›Paper›PMID 20154728›Full record

ArticleOncogene2010

Inhibition of cancer cell proliferation and metastasis by insulin receptor downregulation.

H Zhang, D H Fagan, X Zeng, K T Freeman, D Sachdev, D Yee

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
9.1field-weighted citation impact, top 1% of its field
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

70 citing papers in PubMed, 122 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Obesity: a perfect storm for carcinogenesis.Cancer metastasis reviews · 2022
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Hyperinsulinemia in Obesity, Inflammation, and Cancer.Diabetes & metabolism journal · 2021
    Review
  13. Review
  14. Review
  15. Hyperinsulinaemia in cancer.Nature reviews. Cancer · 2020
    Review
  16. Article
  17. Article
  18. Obesity, Type 2 Diabetes, and Cancer Risk.Frontiers in oncology · 2020
    Review
  19. Article
  20. Article

10 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

H ZhangMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.
D H Fagan
X Zeng
K T Freeman
D Sachdev
D Yee
University of Minnesota · USUniversity of Minnesota Medical Center · US

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
TARGETING THE IGF SYSTEM IN BREAST CANCERR01CA074285 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI YEE, DOUGLAS · 1998 to 2012
$4.0M
NCI NIH HHS P30 CA077598NCI NIH HHS R01 CA074285NCI NIH HHS R01CA74285PHS HHS P30 077598
6 · The paper itself

Abstract

Insulin receptor (IR) and the type I IGF receptor (IGF1R) are structurally and functionally related. The function of IGF1R in cancer has been well documented and anti-IGF1R strategies to treat cancer have shown initial positive results. However, the role of IR in tumor biology, independent of IGF1R, is less clear. To address this issue, short hairpin RNA (shRNA) was used to specifically downregulate IR in two cancer cell lines, LCC6 and T47D. Cells with reduced IR showed reduced insulin-stimulated Akt activation, without affecting IGF1R activation. Cells with reduced IR formed fewer colonies in anchorage-independent conditions. LCC6 IR shRNA xenograft tumors in mice had reduced growth, angiogenesis and lymphangiogensis when compared with LCC6 wild-type cells. Accordingly, LCC6 IR shRNA clones produced less hypoxia-inducible factor-1alpha, vascular endothelial growth factor (VEGF)-A and VEGF-D. Furthermore, LCC6 IR shRNA cells formed fewer pulmonary metastases when compared with LCC6 wild-type cells. Using in vivo luciferase imaging, we have shown that LCC6 IR shRNA cells have less seeding and colonization potential in the lung and liver of mice than LCC6 cells. In conclusion, downregulation of IR inhibited cancer cell proliferation, angiogenesis, lymphangiogenesis and metastasis. Our data argue that IR should also be targeted in cancer therapy.

Indexed as

AnimalsCell Line, TumorCell ProliferationFemaleHumansInsulinLung NeoplasmsLymphangiogenesisMiceNeoplasm MetastasisNeoplasms, ExperimentalNeovascularization, PathologicPhosphorylationProto-Oncogene Proteins c-aktReceptor, InsulinRNA, Small InterferingInsulinProto-Oncogene Proteins c-aktReceptor, InsulinRNA, Small InterferingVascular Endothelial Growth Factor A

Identifiers

PMID20154728
PMCPMC2861724
OpenAlexW1988584992

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.