Evidence map›Paper›PMID 28875407›Full record

ArticleJournal of cancer research and clinical oncology2017

Karyopherin α-2 is a reliable marker for identification of patients with high-risk stage II colorectal cancer.

Dongjun Jeong, Hyeongjoo Kim, Seona Ban, Seunghyun Oh, Sanghee Ji, Doyeon Kim, Tae Sung Ahn, Han Jo Kim, Sang Byung Bae, Hyog Young Kwon and 5 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

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  10. KPNA2 promotes metabolic reprogramming in glioblastomas by regulation of c-myc.Journal of experimental & clinical cancer research : CR · 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

15 authors at 1 institution in 1 country.

Dongjun JeongDepartment of Pathology, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Hyeongjoo KimSoonchunhyang Medical Science Research Institute, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Seona BanSoonchunhyang Medical Science Research Institute, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Seunghyun OhSoonchunhyang Medical Science Research Institute, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Sanghee JiSoonchunhyang Medical Science Research Institute, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Doyeon KimSoonchunhyang Medical Science Research Institute, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Tae Sung AhnDepartment of Surgery, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 330-723, Republic of Korea.
Han Jo KimDepartment of Oncology, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Sang Byung BaeDepartment of Oncology, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Hyog Young KwonDepartment of Pathology, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Jungkyun ImDepartment of Nanochemical Engineering, Soonchunhyang University, 22 Soonchunhyangro, Shinchang-myeon, Asansi, Chungcheongnam-do, 31536, Republic of Korea.
Moon Soo LeeDepartment of Surgery, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 330-723, Republic of Korea.
Hyun Deuk ChoDepartment of Pathology, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Chang-Jin KimDepartment of Pathology, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Moo-Jun BaekDepartment of Surgery, College of Medicine, Soonchunhyang University, 31 Soonchunhyang 6 gil, Dongnam-gu, Cheonan, Chungcheongnam-do, 330-723, Republic of Korea. ssurge@sch.ac.kr.ORCID http://orcid.org/0000-0001-8180-5668
Soonchunhyang University · KR

Funding

National Research Foundation of Korea (KR) 2015R1D1A3A01016798
6 · The paper itself

Abstract

purposeAdjuvant chemotherapy (AC) is frequently considered in patients with high-risk stage II colorectal cancer (CRC). Among patients with stage II CRC who do not receive AC because they are not considered to be at high risk, 20-25% will develop recurrence and die from the disease. Elevated levels of KPNA2 have been observed in various cancers, and overexpression of KPNA2 is related to CRC progression.

methodsWe examined the expression of KPNA2 using 293 CRC tissues, including 118 with stage II CRC, and investigated the applicability of KPNA2 as a biomarker to predict high-risk stage II CRC. Moreover, we further investigated the role of KPNA2 as an oncogene in CRC carcinogenesis using in vitro functional studies.

resultsHigh KPNA2 expression was associated with vascular (p = 0.027) and lymphatic invasion (p = 0.009) in patients with stage II CRC. On multivariate analysis, high KPNA2 expression (HR 3.174, 95% CI 2.060-4.889; p < 0.001) was independently associated with survival in patients with CRC. The overall survival rate in patients with high KPNA2 expression was higher than that in patients with low KPNA2 expression in CRC (p < 0.001), even in patients with stage II CRC (p = 0.001). Additionally, KPNA2 was associated with tumorigenesis and cancer progression in CRC cells; high KPNA2 expression was associated with increased cell proliferation (p < 0.05), migration (p = 0.03), invasion (p = 0.001), and semisolid agar colony formation (p < 0.001).

conclusionKPNA2 expression is useful for identification of patients with high-risk stage II CRC who could benefit from AC and that KPNA2 may also be a promising therapeutic target.

Indexed as

alpha KaryopherinsBiomarkers, TumorCell Line, TumorCell MovementCell ProliferationChemotherapy, AdjuvantColorectal NeoplasmsDown-RegulationFemaleHCT116 CellsHT29 CellsHumansImmunohistochemistryMaleMiddle AgedNeoplasm Stagingalpha KaryopherinsBiomarkers, TumorKPNA2 protein, humanRNA, Small InterferingColorectal cancerCRC stage IIKPNA2Prognostic marker

Identifiers

PMID28875407
PMCPMC11818971
OpenAlexW2753700560

What OpenQuestion holds

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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.