Evidence map›Paper›PMID 32830152›Full record

ArticleThe Journal of reproduction and development2020

Expression and functions of cluster of differentiation 9 and 81 in rat mammary epithelial cells.

Kotaro Horiguchi, Saishu Yoshida, Takehiro Tsukada, Takashi Nakakura, Ken Fujiwara, Rumi Hasegawa, Shu Takigami, Shunji Ohsako

Open access · goldAbstract read
In one paragraph

Article in The Journal of reproduction and development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. CD9, a tetraspanin target for cancer therapy?Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  6. 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

8 authors at 5 institutions in 1 country.

Kotaro HoriguchiLaboratory of Anatomy and Cell Biology, Department of Health Sciences, Kyorin University, Tokyo 181-8612, Japan.
Saishu YoshidaDepartment of Biochemistry, The Jikei University School of Medicine, Tokyo 105-8461, Japan.
Takehiro TsukadaDepartment of Biomolecular Science, Faculty of Science, Toho University, Chiba 274-8510, Japan.
Takashi NakakuraDepartment of Anatomy, Graduate School of Medicine, Teikyo University, Tokyo 173-8605, Japan.
Ken FujiwaraDepartment of Biological Science, Kanagwa University, Kanagawa 259-1293, Japan.
Rumi HasegawaLaboratory of Anatomy and Cell Biology, Department of Health Sciences, Kyorin University, Tokyo 181-8612, Japan.
Shu TakigamiLaboratory of Anatomy and Cell Biology, Department of Health Sciences, Kyorin University, Tokyo 181-8612, Japan.
Shunji OhsakoLaboratory of Anatomy and Cell Biology, Department of Health Sciences, Kyorin University, Tokyo 181-8612, Japan.
Kyorin University · JPJikei University School of Medicine · JPKanagawa University · JPTeikyo University · JPToho University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cluster of differentiation (CD) 9 and CD81 are closely-related members of the tetraspanin family that consist of four-transmembrane domain proteins. Cd9 and Cd81 are highly expressed in breast cancer cells; however, their expression in healthy mammary glands is unclear. In this study, we performed quantitative real-time PCR to analyze the expression levels of Cd9 and Cd81. Histological techniques were employed to identify Cd9- and Cd81-expressing cells in rat mammary glands during pregnancy and lactation. It was observed that Cd9 and Cd81 were expressed in the mammary glands, and their expression levels correlated with mammary gland development. To identify cells expressing Cd9 and Cd81 in the mammary glands, we performed double immunohistochemical staining for CD9 and CD81, prolactin receptor long form, estrogen receptor alpha, or Ki67. The results showed that CD9 and CD81 were co-expressed in proliferating mammary epithelial cells. Next, we attempted to isolate CD9-positive epithelial cells from the mammary gland using pluriBead cell-separation technology based on antibody-mediated binding of cells to beads of different sizes, followed by isolation using sieves with different mesh sizes. We successfully isolated CD9-positive epithelial cells with 96.8% purity. In addition, we observed that small-interfering RNAs against Cd9 and Cd81 inhibited estrogen-induced proliferation of CD9-positive mammary epithelial cells. Our current findings may provide novel insights into the proliferation of mammary epithelial cells during pregnancy and lactation as well as in pathological processes associated with breast cancer.

Indexed as

Gene Expression ProfilingAnimalsCell DifferentiationCell ProliferationDiethylstilbestrolEpithelial CellsEstrogen Receptor alphaFemaleKi-67 AntigenLactationMammary Glands, AnimalPregnancyPregnancy, AnimalRatsRats, WistarReal-Time Polymerase Chain ReactionDiethylstilbestrolEstrogen Receptor alphaKi-67 AntigenRNA, Small InterferingTetraspanin 28Tetraspanin 29CD81Cluster of differentiation (CD) 9LactationMammary glandProliferation

Identifiers

PMID32830152
PMCPMC7768173
OpenAlexW3081366506

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.