Evidence map›Paper›PMID 36380877›Full record

ArticleOncology letters2022

Potential of blood exosomal ENAH, SEPT9, EGF, MMP-9 and CXCL8 for the early screening of breast cancer.

Zijing Zhang, Hongying Wang, Yiting Jin, Chengyu Chu, Jinsong Bai, Juntian Huang, Lemei Yang, Feng Tang, Liping Zou, Shuyang Wang and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2022. 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
0.2field-weighted citation impact, top 51% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  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

11 authors at 3 institutions in 1 country.

Zijing ZhangDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai 200040, P.R. China.
Hongying WangDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai 200040, P.R. China.
Yiting JinDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai 200040, P.R. China.
Chengyu ChuDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai 200040, P.R. China.
Jinsong BaiDepartment of Clinical Medicine, Shanghai Medical College, Fudan University, Shanghai 200433, P.R. China.
Juntian HuangDepartment of Clinical Medicine, Shanghai Medical College, Fudan University, Shanghai 200433, P.R. China.
Lemei YangDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai 200032, P.R. China.
Feng TangDepartment of Pathology, Huashan Hospital, Fudan University, Shanghai 200040, P.R. China.
Liping ZouDepartment of Pathology, Huashan Hospital, Fudan University, Shanghai 200040, P.R. China.
Shuyang WangDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai 200032, P.R. China.
Qiang ZouDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai 200040, P.R. China.
Fudan University · CNShanghai Medical College of Fudan University · CNHuashan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomal contents have been recognized as candidate biomarkers for cancer screening and prognosis. The current study aimed to evaluate the potential of the expression levels of exosomal enabled homolog (ENAH), septin 9 (SEPT9), epidermal growth factor (EGF), matrix metalloproteinase-9 (MMP-9) and C-X-C motif chemokine ligand 8 (CXCL8) in the blood for the early screening of breast cancer. Therefore, exosomes were extracted and purified from the peripheral blood of 47 patients with breast cancer, 63 disease controls (DCs) and 33 healthy controls (HCs). Subsequently, the exosomal mRNA expression levels of ENAH, SEPT9, EGF, MMP-9 and CXCL8 were detected by reverse transcription-quantitative polymerase chain reaction. The results showed that the exosomal levels of ENAH and EGF were significantly higher in patients with breast cancer compared with DCs and HCs (both P<0.001). In addition, receiver operating characteristic curves revealed that exosomal ENAH was able to discriminate patients with breast cancer from DCs [area under the curve (AUC), 0.841] and HCs (AUC, 0.859). However, exosomal EGF was only able to discriminate patients with breast cancer from HCs (AUC, 0.776). Furthermore, the levels of exosomal SEPT9 were lower in patients with breast cancer compared with DCs and HCs (P=0.021), and exosomal SEPT9 expression levels exhibited good potential in the discrimination of patients with breast cancer from DCs (AUC, 0.717) and HCs (AUC, 0.830). However, no significant difference was detected in exosomal levels of MMP-9 and CXCL8 among the three groups, and these RNAs showed no discriminative ability. In addition, in patients with breast cancer, the exosomal levels of ENAH were associated with molecular subtypes (P=0.010), while those of MMP-9 were associated with a Ki-67 index of ≥30% (P=0.011). In conclusion, the exosomal levels of ENAH, SEPT9 and EGF in blood samples were able to identify patients with breast cancer, thus providing a novel approach for the early screening of breast cancer.

Indexed as

breast cancerearly screeningexosomal EGFexosomal ENAHexosomal SEPT9

Identifiers

PMID36380877
PMCPMC9650598
OpenAlexW4308104520

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.