Evidence map›Paper›PMID 30742741›Full record

ArticleCancer science2019

Intraflagellar transport 20 promotes collective cancer cell invasion by regulating polarized organization of Golgi-associated microtubules.

Tomoaki Aoki, Michiru Nishita, Junya Sonoda, Taro Ikeda, Yoshihiro Kakeji, Yasuhiro Minami

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. RGMb drives macrophage infiltration to aggravate kidney disease.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Cancer metabolism and carcinogenesis.Experimental hematology & oncology · 2024
    Review
  5. Article
  6. Review
  7. The Green Valley ofCells · 2022
    Review
  8. Article
  9. Actin-driven Golgi apparatus dispersal during collective migration of epithelial cells.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. 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

6 authors at 1 institution in 1 country.

Tomoaki AokiDivision of Cell Physiology, Department of Physiology and Cell biology, Graduate School of Medicine, Kobe University, Kobe, Japan.
Michiru NishitaDivision of Cell Physiology, Department of Physiology and Cell biology, Graduate School of Medicine, Kobe University, Kobe, Japan.
Junya SonodaDivision of Cell Physiology, Department of Physiology and Cell biology, Graduate School of Medicine, Kobe University, Kobe, Japan.
Taro IkedaDivision of Cell Physiology, Department of Physiology and Cell biology, Graduate School of Medicine, Kobe University, Kobe, Japan.
Yoshihiro KakejiDivision of Gastrointestinal Surgery, Department of Surgery, Graduate School of Medicine, Kobe University, Kobe, Japan.
Yasuhiro MinamiDivision of Cell Physiology, Department of Physiology and Cell biology, Graduate School of Medicine, Kobe University, Kobe, Japan.ORCID https://orcid.org/0000-0003-3514-4285
Kobe University · JP

Funding

Japan Agency for Medical Research and Development 18gm5010001s0901Japan Society for the Promotion of ScienceMinistry of Education, Culture, Sports, Science and Technology 16H05152Mitsubishi Foundation ID 29145
6 · The paper itself

Abstract

Collective invasion is an important strategy of cancers of epithelial origin, including colorectal cancer (CRC), to infiltrate efficiently into local tissues as collective cell groups. Within the groups, cells at the invasive front, called leader cells, are highly polarized and motile, thereby providing the migratory traction that guides the follower cells. However, its underlying mechanisms remain unclear. We have previously shown that signaling emanating from the receptor tyrosine kinase Ror2 can promote invasion of human osteosarcoma cells and that intraflagellar transport 20 (IFT20) mediates its signaling to regulate Golgi structure and transport. Herein, we investigated the role of Ror2 and IFT20 in collective invasion of CRC cells, where Ror2 expression is either silenced or nonsilenced. We show by cell biological analyses that IFT20 promotes collective invasion of CRC cells, irrespective of expression and function of Ror2. Intraflagellar transport 20 is required for organization of Golgi-associated, stabilized microtubules, oriented toward the direction of invasion in leader cells. Our results also indicate that IFT20 promotes reorientation of the Golgi apparatus toward the front side of leader cells. Live cell imaging of the microtubule plus-end binding protein EB1 revealed that IFT20 is required for continuous polarized microtubule growth in leader cells. These results indicate that IFT20 plays an important role in collective invasion of CRC cells by regulating organization of Golgi-associated, stabilized microtubules and Golgi polarity in leader cells.

Indexed as

Carrier ProteinsCell Line, TumorCell MovementGene ExpressionGolgi ApparatusHumansMicrotubulesNeoplasmsReceptor Tyrosine Kinase-like Orphan ReceptorsRNA, Small InterferingCarrier ProteinsIFT20 protein, humanReceptor Tyrosine Kinase-like Orphan ReceptorsRNA, Small InterferingROR2 protein, humancollective invasioncolorectal cancerIFT20noncentrosomal microtubuleRor2

Identifiers

PMID30742741
PMCPMC6447847
OpenAlexW2911990994

What OpenQuestion holds

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LicenceCC BY-NC
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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.