Evidence map›Paper›PMID 27119734›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2017

Downregulated ECRG4 is correlated with lymph node metastasis and predicts poor outcome for nasopharyngeal carcinoma patients.

J-Y Chen, X Wu, C-Q Hong, J Chen, X-L Wei, L Zhou, H-X Zhang, Y-T Huang, L Peng

Abstract read
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In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 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
0.7field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

J-Y ChenOncological Research Lab, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong, People's Republic of China.
X WuOncological Research Lab, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong, People's Republic of China.
C-Q HongOncological Research Lab, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong, People's Republic of China.
J ChenDepartment of Radiotherapy, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong, People's Republic of China.
X-L WeiDepartment of Pathology, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong, People's Republic of China.
L ZhouDepartment of Gynecologic Surgery, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong, People's Republic of China.
H-X ZhangHealth Care Center, The First Affiliated Hospital of Shantou University Medical College, 3/F, Science and Education Building, 52 Southern Dongxia Road, Shantou, 515041, Guangdong Province, People's Republic of China.
Y-T HuangHealth Care Center, The First Affiliated Hospital of Shantou University Medical College, 3/F, Science and Education Building, 52 Southern Dongxia Road, Shantou, 515041, Guangdong Province, People's Republic of China. g_ythuang@stu.edu.cn.
L PengClinical Laboratory, Cancer Hospital of Shantou University Medical College, No. 7 Raoping Road, Shantou, Guangdong, 515041, People's Republic of China. st_penglin@126.com.
Shantou University · CNCancer Hospital of Shantou University Medical College · CNFirst Affiliated Hospital of Shantou University Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveEsophageal cancer-related gene 4 (ECRG4) is a new candidate tumor suppressor gene. In this retrospective study, we evaluated ECRG4 protein expression in patients with nasopharyngeal carcinoma (NPC) under curative treatment and examined its association with pathological features and clinical outcomes as a possible biomarker for diagnosis and prognosis of NPC.

methodsWe enrolled 122 patients with a first diagnosis between January 2001 and December 2003. Tumor tissue and control tissue from biopsies underwent immunohistochemical staining for ECRG4. ECRG4 expression was analyzed by clinicopathological variables. After Kaplan-Meier survival analysis, we used Cox proportional hazards regression to estimate the predictive effect of ECRG4 expression on overall survival.

resultsECRG4 protein level was lower in NPC than control tissue (P < 0.01). It was inversely related to node status (P < 0.001) and clinical stage (P = 0.027). ECRG4 expression was associated with overall survival, and downregulated ECRG4 expression was an independent prognostic factor of poor survival (hazard ratio = 0.677, 95 % confidence interval 0.463-0.989, P = 0.044).

conclusionsA significant NPC patients showed downregulated ECRG4 expression, which is correlated with lymph node metastasis. The marker could be an independent prognostic factor for NPC patients. The precise function of ECRG4 in the progression of NPC, especially for lymphatic metastasis, deserves further investigation, which would bring a new target for personalized therapy.

Indexed as

AdolescentAdultAgedBiomarkers, TumorCarcinomaCombined Modality TherapyFemaleFollow-Up StudiesHumansImmunoenzyme TechniquesLymphatic MetastasisMaleMiddle AgedNasopharyngeal CarcinomaNasopharyngeal NeoplasmsNeoplasm ProteinsBiomarkers, TumorECRG4 protein, humanNeoplasm ProteinsTumor Suppressor ProteinsEsophageal cancer-related gene 4Lymphatic metastasisNasopharyngeal carcinomaPrognostic biomarkerSurvival analysis

Identifiers

PMID27119734
OpenAlexW2344789869

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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.