Evidence map›Paper›PMID 31818360›Full record

ArticleBMB reports2019

TOMM20 as a potential therapeutic target of colorectal cancer.

Sang-Hee Park, Ah-Reum Lee, Keonwoo Choi, Soyoung Joung, Jong-Bok Yoon, Sungjoo Kim

Open access · goldAbstract read
In one paragraph

Article in BMB reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 84 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

6 authors at 2 institutions in 1 country.

Sang-Hee ParkDepartment of Biomedicine & Health Sciences, Graduate School, The Catholic University of Korea, Seoul 05535; Department of Medical Life Sciences, College of Medicine, The Catholic University of Korea, Seoul 05535, Korea.
Ah-Reum LeeDepartment of Biomedicine & Health Sciences, Graduate School, The Catholic University of Korea, Seoul 05535; Department of Medical Life Sciences, College of Medicine, The Catholic University of Korea, Seoul 05535, Korea.
Keonwoo ChoiDepartment of Biomedicine & Health Sciences, Graduate School, The Catholic University of Korea, Seoul 05535; Department of Medical Life Sciences, College of Medicine, The Catholic University of Korea, Seoul 05535, Korea.
Soyoung JoungDepartment of Biomedicine & Health Sciences, Graduate School, The Catholic University of Korea, Seoul 05535; Department of Medical Life Sciences, College of Medicine, The Catholic University of Korea, Seoul 05535, Korea.
Jong-Bok YoonDepartment of Biochemistry, College of Life Science & Biotechnology, Yonsei University, Seoul 05535, Korea.
Sungjoo KimDepartment of Medical Life Sciences, College of Medicine, The Catholic University of Korea, Seoul 05535, Korea.
Catholic University of Korea · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Translocase of outer mitochondrial membrane 20 (TOMM20) plays an essential role as a receptor for proteins targeted to mitochondria. TOMM20 was shown to be overexpressed in various cancers. However, the oncological function and therapeutic potential for TOMM20 in cancer remains largely unexplored. The purpose of this study was to elucidate the underlying molecular mechanism of TOMM20's contribution to tumorigenesis and to explore the possibility of its therapeutic potential using colorectal cancer as a model. The results show that TOMM20 overexpression resulted in an increase in cell proliferation, migration, and invasion of colorectal cancer (CRC) cells, while siRNA-mediated inhibition of TOMM20 resulted in significant decreases in cell proliferation, migration, and invasion. TOMM20 expression directly impacted the mitochondrial function including ATP production and maintenance of membrane potential, which contributed to tumorigenic cellular activities including regulation of S phase cell cycle and apoptosis. TOMM20 was overexpressed in CRC compared to the normal tissues and increased expression of TOMM20 to be associated with malignant characteristics including a higher number of lymph nodes and perineural invasion in CRC. Notably, knockdown of TOMM20 in the xenograft mouse model resulted in a significant reduction of tumor growth. This is the first report demonstrating a relationship between TOMM20 and tumorigenesis in colorectal cancer and providing promising evidence for the potential for TOMM20 to serve as a new therapeutic target of colorectal cancer. [BMB Reports 2019; 52(12): 712-717].

Indexed as

Adenosine TriphosphateAnimalsApoptosisCarcinogenesisCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsGene Expression Regulation, NeoplasticHumansMembrane Potential, MitochondrialMembrane Transport ProteinsMiceMice, Inbred BALB CMice, NudeMiddle AgedAdenosine TriphosphateMembrane Transport ProteinsMitochondrial Precursor Protein Import Complex ProteinsReceptors, Cell SurfaceTOMM20 protein, human

Identifiers

PMID31818360
PMCPMC6941759
OpenAlexW2998620589

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.