Evidence map›Paper›PMID 32526706›Full record

ArticleAging2020

ANXA7 promotes the cell cycle, proliferation and cell adhesion-mediated drug resistance of multiple myeloma cells by up-regulating CDC5L.

Haiyan Liu, Dan Guo, Yuou Sha, Chenlu Zhang, Yijing Jiang, Lemin Hong, Jie Zhang, Yuwen Jiang, Ling Lu, Hongming Huang

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. CAM-DR: Mechanisms, Roles and Clinical Application in Tumors.Frontiers in cell and developmental biology · 2021
    Review
  14. Annexin A7 Regulates Endometrial Receptivity.Frontiers in cell and developmental biology · 2020
    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

10 authors at 3 institutions in 1 country.

Haiyan LiuDepartment of Hematology, The Affiliated Hospital of Nantong University, Nantong 226001, China.
Dan GuoDepartment of Hematology, The Affiliated Hospital of Nantong University, Nantong 226001, China.
Yuou ShaSchool of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Chenlu ZhangDepartment of Hematology, The Affiliated Hospital of Nantong University, Nantong 226001, China.
Yijing JiangDepartment of Hematology, The Affiliated Hospital of Nantong University, Nantong 226001, China.
Lemin HongDepartment of Hematology, The Affiliated Hospital of Nantong University, Nantong 226001, China.
Jie ZhangDepartment of Hematology, The Affiliated Hospital of Nantong University, Nantong 226001, China.
Yuwen JiangDepartment of Hematology, The Affiliated Hospital of Nantong University, Nantong 226001, China.
Ling LuDepartment of Hematology, The Affiliated Hospital of Nantong University, Nantong 226001, China.
Hongming HuangDepartment of Hematology, The Affiliated Hospital of Nantong University, Nantong 226001, China.
Nantong University · CNAffiliated Hospital of Nantong University · CNHuazhong University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to investigate whether annexin A7 (ANXA7) could promote the cell cycle, proliferation and cell adhesion-mediated drug resistance (CAM-DR) of multiple myeloma (MM) cells by up-regulating cell division cycle 5-like (CDC5L). As a result, ANXA7 expression was increased in the serum of MM patients and the expression of ANXA7 and CDC5L was also increased in MM cell lines. ANXA7 overexpression promoted the proliferation and cycle of U266 and RPMI8226 cells. The expression of proliferation cell nuclear antigen (PCNA), KI67, cyclin dependent kinase 1 (CDK1) and cyclinB1 in transfected cells was consistent with the changes of proliferation and cell cycle. In co-culture system of BMSC cells and MM cells, expression of CD44, ICAM1 and VCAM1 in MM cells was increased, which was further increased by ANXA7 overexpression. Bortezomib could increase the apoptosis of U266 and RPMI8226 cells. In co-culture system of BMSC cells and MM cells, the promotion effects of bortezomib on apoptosis of MM cells was decreased, which was further suppressed by ANXA7 overexpression. The above effects exerted by ANXA7 overexpression could be reversed by ANXA7 interference. Moreover, ANXA7 was proved to be combined with CDC5L. CDC5L interference could inhibit the promotion effects of ANXA7 overexpression on proliferation and cell cycle and inhibition effects of ANXA7 overexpression on apoptosis of MM cells treated with bortezomib in co-culture system. In conclusion, ANXA7 could promote the cell cycle, proliferation and CAM-DR of MM cells by up-regulating CDC5L.

Indexed as

Drug Resistance, NeoplasmAnnexin A7Antineoplastic AgentsApoptosisBortezomibCell AdhesionCell CycleCell Cycle ProteinsCell Line, TumorCell ProliferationCoculture TechniquesHumansMultiple MyelomaRNA-Binding ProteinsUp-RegulationAnnexin A7Antineoplastic AgentsBortezomibCDC5L protein, humanCell Cycle ProteinsRNA-Binding ProteinsANXA7CDC5Lcell cycledrug resistancemultiple myeloma

Identifiers

PMID32526706
PMCPMC7346058
OpenAlexW3034876561

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.