Inositol (1,4,5)-Trisphosphate Receptors in Invasive Breast Cancer: A New Prognostic Tool?

被引:7
|
作者
Foulon, Arthur [1 ,2 ]
Rybarczyk, Pierre [2 ,3 ]
Jonckheere, Nicolas [4 ]
Brabencova, Eva [5 ]
Sevestre, Henri [2 ,3 ]
Ouadid-Ahidouch, Halima [2 ]
Rodat-Despoix, Lise [2 ]
机构
[1] Univ Picardie Jules Verne, Ctr Gynecol Obstet, CHU Amiens Picardie, F-80089 Amiens, France
[2] Univ Picardie Jules Verne, Lab Physiol Cellulaire & Mol, UR UPJV 4667, F-80090 Amiens, France
[3] Univ Picardie Jules Verne, Serv Anat & Cytol Pathol, CHU Amiens Picardie, F-80090 Amiens, France
[4] Univ Lille, CHU Lille, CANTHER Canc Heterogene Plast & Resistance Therap, CNRS,Inserm,UMR9020,U1277, F-59000 Lille, France
[5] Ctr Lutte Canc Reims & Champagne Ardenne, Ctr Ressources Biol, Jean Godinot Inst Canc Ctr, F-51100 Reims, France
关键词
inositol; 1; 4; 5; trisphosphate; breast cancer; invasive prognostic marker; 1,4,5-TRISPHOSPHATE RECEPTOR; HER-2/NEU AMPLIFICATION; LOCOREGIONAL RECURRENCE; EXPRESSION; METASTASIS; SURVIVAL; TUMOR; APOPTOSIS; C-ERBB-2; SUBTYPES;
D O I
10.3390/ijms23062962
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Simple Summary The inositol-trisphosphate receptor (IP3R) is a key player in physiological and pathological intracellular calcium signaling. The objective of the present study was to assess the putative value of the three IP3R subtypes as prognostic biomarkers in breast cancer. We found that IP(3)R3 is the most strongly expressed subtype in breast cancer tissue. Furthermore, IP(3)R3 and IP(3)R1 are significantly more expressed in invasive breast cancer tissue than in non-tumor tissue. In contrast to IP(3)R1 and IP(3)R2, the expression of IP(3)R3 was positively correlated with prognostic factors including tumor size, regional node invasion, histologic grade, proliferation index, and hormonal status. By analyzing public databases, we found that the expression of all IP3R subtypes is significantly correlated with the overall survival and disease-free survival of patients with breast cancer. We conclude that relative to the other two IP3R subtypes, IP(3)R3 expression is upregulated in breast cancer and is correlated with prognostic factors. We strongly believe that our results will open up new perspectives with regard to the link between IP(3)Rs and breast cancer aggressiveness. Breast cancer is the leading cause of cancer death among women in worldwide and France. The disease prognosis and treatment differ from one breast cancer subtype to another, and the disease outcome depends on many prognostic factors. Deregulation of ion flux (especially Ca2+ flux) is involved in many pathophysiology processes, including carcinogenesis. Inside the cell, the inositol-trisphosphate receptor (IP3R) is a major player in the regulation of the Ca2+ flux from the endoplasmic reticulum to the cytoplasm. The IP(3)Rs (and particularly the IP(3)R3 subtype) are known to be involved in proliferation, migration, and invasion processes in breast cancer cell lines. The objective of the present study was to evaluate the potential value of IP(3)Rs as prognostic biomarkers in breast cancer. We found that expression levels of IP(3)R3 and IP(3)R1 (but not IP(3)R2) were significantly higher in invasive breast cancer of no special type than in non-tumor tissue from the same patient. However, the IP(3)R3 subtype was expressed more strongly than the IP(3)R1 and IP(3)R2 subtypes. Furthermore, the expression of IP(3)R3 (but not of IP(3)R1 or IP(3)R2) was positively correlated with prognostic factors such as tumor size, regional node invasion, histologic grade, proliferation index, and hormone receptor status. In an analysis of public databases, we found that all IP(3)Rs types are significantly associated with overall survival and progression-free survival in patients with breast cancer. We conclude that relative to the other two IP3R subtypes, IP(3)R3 expression is upregulated in breast cancer and is correlated with prognostic factors.
引用
收藏
页数:17
相关论文
共 50 条
  • [21] Inositol 1,4,5-trisphosphate signaling maintains the activity of glutamate uptake in Bergmann glia
    Mashimo, Masato
    Okubo, Yohei
    Yamazawa, Toshiko
    Yamasaki, Miwako
    Watanabe, Masahiko
    Murayama, Toshihiko
    Iino, Masamitsu
    EUROPEAN JOURNAL OF NEUROSCIENCE, 2010, 32 (10) : 1668 - 1677
  • [22] The type III inositol 1,4,5-trisphosphate receptor is associated with aggressiveness of colorectal carcinoma
    Shibao, Kazunori
    Fiedler, Michael J.
    Nagata, Jun
    Minagawa, Noritaka
    Hirata, Keiji
    Nakayama, Yoshifumi
    Iwakiri, Yasuko
    Nathanson, Michael H.
    Yamaguchi, Koji
    CELL CALCIUM, 2010, 48 (06) : 315 - 323
  • [23] Inositol 1,4,5-trisphosphate 3-kinases:functions and regulations
    Hui Jun XIA*
    CellResearch, 2005, (02) : 83 - 91
  • [24] The BRCA1 Tumor Suppressor Binds to Inositol 1,4,5-Trisphosphate Receptors to Stimulate Apoptotic Calcium Release
    Hedgepeth, Serena C.
    Garcia, M. Iveth
    Wagner, Larry E., II
    Rodriguez, Ana M.
    Chintapalli, Sree V.
    Snyder, Russell R.
    Hankins, Gary D. V.
    Henderson, Beric R.
    Brodie, Kirsty M.
    Yule, David I.
    van Rossum, Damian B.
    Boehning, Darren
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290 (11) : 7304 - 7313
  • [25] Regulation of the cerebellar inositol 1,4,5-trisphosphate receptor by univalent cations
    Coquil, JF
    Blazquez, S
    Soave, S
    Mauger, JP
    BIOCHEMICAL JOURNAL, 2004, 381 : 423 - 428
  • [26] Gene Knock-Outs of Inositol 1,4,5-Trisphosphate Receptors Types 1 and 2 Result in Perturbation of Cardiogenesis
    Uchida, Keiko
    Aramaki, Megumi
    Nakazawa, Maki
    Yamagishi, Chihiro
    Makino, Shinji
    Fukuda, Keiichi
    Nakamura, Takeshi
    Takahashi, Takao
    Mikoshiba, Katsuhiko
    Yamagishi, Hiroyuki
    PLOS ONE, 2010, 5 (09): : 1 - 10
  • [27] Inositol 1,4,5-trisphosphate receptor type 3 is involved in resistance to apoptosis and maintenance of human hepatocellular carcinoma
    Dos Santos, Marcone Loiola
    Franca, Andressa
    Melo Lima Filho, Antonio Carlos
    Florentino, Rodrigo M.
    Diniz, Paulo Henrique
    Lemos, Fernanda Oliveira
    Xavier Goncalves, Carlos Alberto
    Coelho, Vitor Lima
    Lima, Cristiano Xavier
    Foureaux, Giselle
    Nathanson, Michael H.
    Teixeira Vidigal, Paula Vieira
    Fatima Leite, M.
    ONCOLOGY LETTERS, 2022, 23 (01)
  • [28] Unique Regulatory Properties of Heterotetrameric Inositol 1,4,5-Trisphosphate Receptors Revealed by Studying Concatenated Receptor Constructs
    Chandrasekhar, Rahul
    Alzayady, Kamil J.
    Wagner, Larry E., II
    Yule, David I.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291 (10) : 4846 - 4860
  • [29] Highly Sensitive Measurement of Inositol 1,4,5-Trisphosphate by Using a New Fluorescent Ligand and Ligand Binding Domain Combination
    Oura, Tai
    Murata, Kaori
    Morita, Takao
    Nezu, Akihiro
    Arisawa, Mitsuhiro
    Shuto, Satoshi
    Tanimura, Akihiko
    CHEMBIOCHEM, 2016, 17 (16) : 1509 - 1512
  • [30] INOSITOL AND INOSITOL 1,4,5-TRISPHOSPHATE CONTENT OF DOWN-SYNDROME FIBROBLASTS EXHIBITING ENHANCED INOSITOL UPTAKE
    FRUEN, BR
    LESTER, BR
    FEBS LETTERS, 1991, 295 (1-3): : 43 - 47