Evidence map›Paper›PMID 26807311›Full record

ArticleAmerican journal of cancer research2015

Impact of prospero homeobox-1 on tumor cell behavior and prognosis in colorectal cancer.

Young-Lan Park, Eun Myung, Sun-Young Park, Nuri Kim, Chan-Young Oak, Dae-Seong Myung, Sung-Bum Cho, Wan-Sik Lee, Sun-Seog Kweon, Hyun-Soo Kim and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. PROX1-mediated epigenetic silencing ofInternational journal of biological sciences · 2023
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
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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

11 authors at 1 institution in 1 country.

Young-Lan ParkDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Eun MyungDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Sun-Young ParkDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Nuri KimDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Chan-Young OakDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Dae-Seong MyungDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Sung-Bum ChoDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Wan-Sik LeeDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Sun-Seog KweonDepartment of Preventive Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Hyun-Soo KimDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Young-Eun JooDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Chonnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prospero homeobox 1 (PROX1) is up-regulated in colorectal cancer and plays an oncogenic role. In the present study, we sought to investigate the impact of PROX1 on oncogenic processes and to assess the prognostic value of PROX1 expression in colorectal cancer. A small interfering RNA or pcDNA6-myc vector was used to control PROX1 gene expression in colorectal cancer DLD1 and SW480 cell lines. The expression of PROX1 in colorectal cancer tissues was investigated by immunohistochemistry. Angiogenesis, lymphangiogenesis, and tumor cell proliferation were assessed by analyzing the expression of respective markers of these phenomena, CD34, D2-40, and Ki-67 after immunohistochemical staining. PROX1 knockdown decreased both umbilical vein endothelial cell invasion and tube formation, down-regulated the expression of VEGF-A and HIF-1α, and up-regulated the expression of angiostatin. Lymphatic endothelial cell invasion and tube formation as well as the expression of VEGF-C were also suppressed by PROX1 knockdown. PROX1 knockdown suppressed tumor cell proliferation, migration, invasion, and epithelial-mesenchymal transition. In contrast, PROX1 overexpression enhanced tumor cell angiogenesis, lymphangiogenesis, proliferation, migration, invasion, and epithelial-mesenchymal transition. Levels of phosphorylated Akt, GSK3β, and MAPK were decreased by PROX1 knockdown and increased by PROX1 overexpression. PROX1 expression positively correlated with tumor size, extent of differentiation, lymphovascular invasion, depth of invasion, lymph node metastasis, stage, and poor survival. The mean microvessel density and Ki-67 labeling index values of PROX1-positive tumors were significantly higher than those of PROX1-negative tumors. However, there was no significant correlation between PROX1 expression and lymphatic vessel density. These results indicate that PROX1 influences tumor progression in colorectal cancer by regulating angiogenesis and tumor cell proliferation.

Indexed as

angiogenesiscolorectal neoplasmprognosisproliferationProspero homeobox 1

Identifiers

PMID26807311
PMCPMC4697677
OpenAlexW2395172160

What OpenQuestion holds

Textmetadata
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.