Evidence map›Paper›PMID 28963677›Full record

ArticleVirchows Archiv : an international journal of pathology2017

HCRP1 downregulation confers poor prognosis and induces chemoresistance through regulation of EGFR-AKT pathway in human gastric cancer.

Hao Xu, Zhi-Feng Miao, Zhen-Ning Wang, Ting-Ting Zhao, Ying-Ying Xu, Yong-Xi Song, Jin-Yu Huang, Jun-Yan Zhang, Xing-Yu Liu, Jian-Hua Wu and 1 more

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. HCRP1, ID4 and Glypican-3: an optimal panel of biomarkers for diagnosis of hepatocellular carcinoma.International journal of clinical and experimental pathology · 2018
    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

11 authors.

Hao XuDepartment of Surgical Oncology, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Zhi-Feng MiaoDepartment of Surgical Oncology, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Zhen-Ning WangDepartment of Surgical Oncology, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Ting-Ting ZhaoDepartment of Breast Surgery, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Ying-Ying XuDepartment of Breast Surgery, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Yong-Xi SongDepartment of Surgical Oncology, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Jin-Yu HuangDepartment of Surgical Oncology, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Jun-Yan ZhangDepartment of Surgical Oncology, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Xing-Yu LiuDepartment of Surgical Oncology, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Jian-Hua WuDepartment of Surgical Oncology, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Hui-Mian XuDepartment of Surgical Oncology, First Hospital of China Medical University, Shenyang, Liaoning Province, China. 13898829926@163.com.

Funding

National Natural Science Foundation of China 81272718National Natural Science Foundation of China 81302125
6 · The paper itself

Abstract

The current study aims to investigate the biological roles and clinical significance of HCRP1 in human gastric cancer. The expression pattern of HCRP1 in gastric cancer tissue and adjacent non-cancerous tissue was detected by immunohistochemistry. HCRP1 downregulation was found in 57 of 137 human gastric cancer samples and correlated with advanced TNM stage, positive nodal status, and relapse. Log-rank test showed that HCRP1 downregulation also correlated with poor overall survival and reduced relapse-free survival. In addition, we found that HCRP1 overexpression inhibited proliferation, colony formation, and invasion in HGC-27 cells. On the other hand, HCRP1 depletion by small interfering RNA promoted proliferation, colony formation, and invasion in SGC-7901 cells. We also treated gastric cancer cells with cisplatin. MTT and Annexin V/PI analysis were carried out to examine change of chemoresistance. We found that HCRP1 overexpression sensitized HGC-27 cells to cisplatin while its depletion reduced sensitivity in SGC-7901 cells. Moreover, we found that HCRP1 overexpression negatively regulated cyclin D1, MMP-2, p-EGFR, p-ERK, and p-AKT. HCRP1 depletion showed the opposite effects. In conclusion, our results suggest that HCRP1 downregulation might serve as an indicator for poor prognosis in gastric cancer patients. HCRP1 reduces drug resistance through regulation of EGFR-AKT signaling.

Indexed as

Signal TransductionAdultAgedDisease-Free SurvivalDown-RegulationDrug Resistance, NeoplasmEndosomal Sorting Complexes Required for TransportErbB ReceptorsFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMaleMiddle AgedPrognosisProto-Oncogene Proteins c-aktEGFR protein, humanEndosomal Sorting Complexes Required for TransportErbB ReceptorsProto-Oncogene Proteins c-aktVPS37A protein, humanCell cycleGastric cancerHCRP1Resistance

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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.