Evidence map›Paper›PMID 38092728›Full record

ArticleNature communications2023

Niacin restriction with NAMPT-inhibition is synthetic lethal to neuroendocrine carcinoma.

Miyuki Nomura, Mai Ohuchi, Yoshimi Sakamoto, Kei Kudo, Keisuke Yaku, Tomoyoshi Soga, Yuki Sugiura, Mami Morita, Kayoko Hayashi, Shuko Miyahara and 19 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 22 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

29 authors at 8 institutions in 1 country.

Miyuki NomuraDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Mai OhuchiDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Yoshimi SakamotoDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Kei KudoDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Keisuke YakuDepartment of Molecular and Medical Pharmacology, Faculty of Medicine, University of Toyama, Toyama, Japan.
Tomoyoshi SogaInstitute for Advanced Biosciences, Keio University, Tsuruoka, Japan.ORCID 0000-0001-9502-2509
Yuki SugiuraCenter for Cancer Immunotherapy and Immunobiology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Mami MoritaDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Kayoko HayashiDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Shuko MiyaharaDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.ORCID 0000-0002-7753-636X
Taku SatoDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Yoji YamashitaDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Shigemi ItoDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Naohiko KikuchiDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Ikuro SatoDepartment of Pathology, Miyagi Cancer Center Hospital, Natori, Japan.
Rintaro SaitoInstitute for Advanced Biosciences, Keio University, Tsuruoka, Japan.
Nobuo YaegashiDepartment of Obstetrics and Gynecology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Tatsuro FukuharaDepartment of Respiratory Medicine, Miyagi Cancer Center Hospital, Natori, Japan.ORCID 0000-0003-0440-470X
Hidekazu YamadaDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Hiroshi ShimaDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan.
Keiichi I NakayamaDepartment of Molecular and Cellular Biology, Medical Institute of Bioregulation, Kyusyu University, Fukuoka, Japan.ORCID 0000-0002-7185-1529
Atsushi HiraoDivision of Molecular Genetics, Cancer and Stem Cell Research Program, Cancer Research Institute and WPI Nano Life Science Institute, Kanazawa University, Kanazawa, Japan.
Kenta KawasakiDepartment of Organoid Medicine, Keio University School of Medicine, Tokyo, Japan.
Yoichi AraiDepartment of Urology, Miyagi Cancer Center Hospital, Natori, Japan.
Shusuke AkamatsuDepartment of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Sei-Ichi TanumaMeikai University Research Institute of Odontology, Sakado, Japan.
Toshiro SatoDepartment of Organoid Medicine, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0001-8353-8137
Takashi NakagawaDepartment of Molecular and Medical Pharmacology, Faculty of Medicine, University of Toyama, Toyama, Japan.ORCID 0000-0001-5539-7605
Nobuhiro TanumaDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Japan. ntanuma@med.tohoku.ac.jp.ORCID 0000-0001-7914-1380
Miyagi Prefectural Hospital Organization · JPKeio University · JPTohoku University · JPKyoto University · JPUniversity of Toyama · JPKanazawa University · JPMeikai University · JPTokyo Medical and Dental University · JP

Funding

Japan Agency for Medical Research and Development (AMED) 23ama221122h0001MEXT | Japan Society for the Promotion of Science (JSPS) 19H01036MEXT | Japan Society for the Promotion of Science (JSPS) 19K09469MEXT | Japan Society for the Promotion of Science (JSPS) 20K17203MEXT | Japan Society for the Promotion of Science (JSPS) 21K09482MEXT | Japan Society for the Promotion of Science (JSPS) 21K16531MEXT | Japan Society for the Promotion of Science (JSPS) 21K19420MEXT | Japan Society for the Promotion of Science (JSPS) 21K19748MEXT | Japan Society for the Promotion of Science (JSPS) 22K08989Princess Takamatsu Cancer Research Fund NA
6 · The paper itself

Abstract

Nicotinamide phosphoribosyltransferase (NAMPT) plays a major role in NAD biosynthesis in many cancers and is an attractive potential cancer target. However, factors dictating therapeutic efficacy of NAMPT inhibitors (NAMPTi) are unclear. We report that neuroendocrine phenotypes predict lung and prostate carcinoma vulnerability to NAMPTi, and that NAMPTi therapy against those cancers is enhanced by dietary modification. Neuroendocrine differentiation of tumor cells is associated with down-regulation of genes relevant to quinolinate phosphoribosyltransferase-dependent de novo NAD synthesis, promoting NAMPTi susceptibility in vitro. We also report that circulating nicotinic acid riboside (NAR), a non-canonical niacin absent in culture media, antagonizes NAMPTi efficacy as it fuels NAMPT-independent but nicotinamide riboside kinase 1-dependent NAD synthesis in tumors. In mouse transplantation models, depleting blood NAR by nutritional or genetic manipulations is synthetic lethal to tumors when combined with NAMPTi. Our findings provide a rationale for simultaneous targeting of NAR metabolism and NAMPT therapeutically in neuroendocrine carcinoma.

Indexed as

Carcinoma, NeuroendocrineNiacinAnimalsCell Line, TumorCytokinesMaleMiceNADNicotinamide PhosphoribosyltransferaseCytokinesNADNiacinNicotinamide Phosphoribosyltransferase

Identifiers

PMID38092728
PMCPMC10719245
OpenAlexW4389676215

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.