Evidence map›Paper›PMID 38900300›Full record

ArticleJournal of gastroenterology2024

Dietary vitamin D intake and risk of colorectal cancer according to vitamin D receptor expression in tumors and their surrounding stroma.

Shiori Nakano, Taiki Yamaji, Akihisa Hidaka, Taichi Shimazu, Kouya Shiraishi, Aya Kuchiba, Masahiro Saito, Fumihito Kunishima, Ryouji Nakaza, Takashi Kohno and 4 more

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Article in Journal of gastroenterology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
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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

14 authors.

Shiori NakanoDivision of Epidemiology, National Cancer Center Institute for Cancer Control, 5-1-1, Tsukiji, Chou-ku, Tokyo, 104-0045, Japan.
Taiki YamajiDivision of Epidemiology, National Cancer Center Institute for Cancer Control, 5-1-1, Tsukiji, Chou-ku, Tokyo, 104-0045, Japan. tyamaji@ncc.go.jp.ORCID 0000-0002-4799-8782
Akihisa HidakaDivision of Epidemiology, National Cancer Center Institute for Cancer Control, 5-1-1, Tsukiji, Chou-ku, Tokyo, 104-0045, Japan.
Taichi ShimazuDivision of Behavioral Sciences, National Cancer Center Institute for Cancer Control, Tokyo, Japan.
Kouya ShiraishiDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
Aya KuchibaGraduate School of Health Innovation, Kanagawa University of Human Services, Kanagawa, Japan.
Masahiro SaitoDepartment of Diagnostic Pathology, Hiraka General Hospital, Yokote, Akita, Japan.
Fumihito KunishimaDepartment of Diagnostic Pathology, Okinawa Prefecture Chubu Hospital, Okinawa, Japan.
Ryouji NakazaDepartment of Clinical Laboratory, Nakagami Hospital, Okinawa, Japan.
Takashi KohnoDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
Norie SawadaDivision of Cohort Research, National Cancer Center Institute for Cancer Control, Tokyo, Japan.
Manami InoueDivision of Prevention, National Cancer Center Institute for Cancer Control, Tokyo, Japan.
Shoichiro TsuganeDivision of Cohort Research, National Cancer Center Institute for Cancer Control, Tokyo, Japan.
Motoki IwasakiDivision of Epidemiology, National Cancer Center Institute for Cancer Control, 5-1-1, Tsukiji, Chou-ku, Tokyo, 104-0045, Japan.

Funding

Japan Agency for Medical Research and Development JP19ck0106266Japan Agency for Medical Research and Development JP22ck0106551Ministry of Health, Labour and Welfare a Grant-in-Aid for Cancer ResearchNational Cancer Center Research and Development Fund 2020-J-2National Cancer Center Research and Development Fund 2020-J-4National Cancer Center Research and Development Fund 23-A-31 [toku]National Cancer Center Research and Development Fund 26-A-2National Cancer Center Research and Development Fund 29-A-4
6 · The paper itself

Abstract

backgroundColorectal Cancer (CRC) has been molecularly classified into several subtypes according to tumor, stromal, and immune components. Here, we investigated whether the preventive effect of vitamin D on CRC varies with subtypes defined by Vitamin D receptor (VDR) expression in tumors and their surrounding stroma, along with the association of somatic mutations in CRC.

methodsIn a population-based prospective study of 22,743 Japanese participants, VDR expression levels in tumors and their surrounding stroma were defined in 507 cases of newly diagnosed CRC using immunohistochemistry. Hazard ratios of CRC and its subtypes according to dietary vitamin D intake were estimated using multivariable Cox proportional hazards models.

resultsDietary vitamin D intake was not associated with CRC or its subtypes defined by VDR expression in tumors. However, an inverse association was observed for CRC with high VDR expression in the stroma (the highest tertile vs the lowest tertile: 0.46 [0.23-0.94], P

conclusionsThis study provides the first evidence that the preventive effect of vitamin D on CRC depends on VDR expression in the stroma rather than in the tumors. CRC with high VDR expression in the stroma is likely to develop through a part of the serrated polyp pathway, which tends to occur with BRAF but not with APC mutations.

Indexed as

Colorectal NeoplasmsMutationProto-Oncogene Proteins B-rafReceptors, CalcitriolVitamin DAgedDietFemaleHumansJapanMaleMiddle AgedProportional Hazards ModelsProspective StudiesTumor Suppressor Protein p53BRAF protein, humanProto-Oncogene Proteins B-rafReceptors, CalcitriolTP53 protein, humanTumor Suppressor Protein p53VDR protein, humanVitamin DColorectal cancerTumor stromaVitamin D intakeVitamin D receptor

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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.