Evidence map›Paper›PMID 32207278›Full record

ArticleEndocrinology and metabolism (Seoul, Korea)2020

Therapeutic Effect of a Novel Chimeric Molecule Targeting Both Somatostatin and Dopamine Receptors on Growth Hormone-Secreting Pituitary Adenomas.

Jean Kim, Ju Hun Oh, Heather Harlem, Michael D Culler, Cheol Ryong Ku, Eun Jig Lee

Open access · diamondAbstract read
In one paragraph

Article in Endocrinology and metabolism (Seoul, Korea), 2020. 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
0.7field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Pituitary Tumorigenesis-Implications for Management.Medicina (Kaunas, Lithuania) · 2023
    Review
  2. Review
  3. 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.

Jean Kim *Brain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, Korea.ORCID 0000-0003-0047-8074
Ju Hun Oh *Brain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, Korea.ORCID 0000-0003-0795-6649
Heather HarlemEndocrinology Research, Ipsen Bioscience Inc., Cambridge, MA, USA.
Michael D CullerEndocrinology Research, Ipsen Bioscience Inc., Cambridge, MA, USA.
Cheol Ryong KuEndocrinology, Institute of Endocrine Research, Yonsei University College of Medicine, Seoul, Korea. cr079@yuhs.ac.ORCID 0000-0001-8693-9630
Eun Jig LeeBrain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, Korea.ORCID 0000-0003-3231-9887
Yonsei University · KR

Funding

MHW HI15C1584NRF NRF-2017R1D1A1B03033587
6 · The paper itself

Abstract

backgroundAcromegaly is a rare disease primarily caused by growth hormone (GH)-secreting pituitary adenomas, and its treatment is costly. Moreover, some patients are unresponsive to treatment. Hence, there are increasing efforts to develop new drugs with improved effectiveness for this disease. BIM23B065 is a novel chimeric molecule that acts on both somatostatin and dopamine receptors. This study aimed to investigate the effects of BIM23B065 compared with those of a somatostatin receptor analog and a dopamine agonist.

methodsThe effects of BIM23B065 on the proliferation, GH and insulin-like growth factor-1 (IGF-1) levels, and extracellular signal-regulated kinase (ERK) 1/2 and cyclic AMP response element binding (CREB) phosphorylation of GH3 cells were investigated with MTS assay, enzyme-linked immunosorbent assay, and Western blotting, respectively. The dosage and treatment duration of BIM23B065 were tested in animal models of GH-secreting pituitary adenoma. The effect of BIM23B065 (3 mg/kg/day) on changes in IGF-1 levels before and after treatment was further investigated.

results

conclusionThe novel chimeric molecule was effective in decreasing IGF-1 and GH levels and may serve as an effective therapeutic agent for acromegaly.

Indexed as

AdenomaAnimalsCell ProliferationDopamineGene Expression Regulation, NeoplasticGrowth Hormone-Secreting Pituitary AdenomaIntracellular Signaling Peptides and ProteinsMaleMiceMice, Inbred C57BLMice, KnockoutRatsReceptors, DopamineReceptors, SomatostatinSomatostatinTumor Cells, Culturedaryl hydrocarbon receptor-interacting proteinBIM23B065DopamineIntracellular Signaling Peptides and ProteinsReceptors, DopamineReceptors, SomatostatinSomatostatinAcromegalyGrowth hormoneInsulin-like growth factor IPituitary neoplasmsTherapeutics

Identifiers

PMID32207278
PMCPMC7090307
OpenAlexW3012913235

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.