1
|
Bellahcène A, Castronovo V, Ogbureke KU,
Fisher LW and Fedarko NS: Small integrin-binding ligand N-linked
glycoproteins (SIBLINGs): Multifunctional proteins in cancer. Nat
Rev Cancer. 8:212–226. 2008. View
Article : Google Scholar : PubMed/NCBI
|
2
|
Ogbureke KU and Fisher LW: Expression of
SIBLINGs and their partner MMPs in salivary glands. J Dent Res.
83:664–670. 2004. View Article : Google Scholar : PubMed/NCBI
|
3
|
Ogbureke KU and Fisher LW: SIBLING
expression patterns in duct epithelia reflect the degree of
metabolic activity. J Histochem Cytochem. 55:403–409. 2007.
View Article : Google Scholar : PubMed/NCBI
|
4
|
Koli K, Saxena G and Ogbureke KU:
Expression of matrix metal-loproteinase (MMP)-20 and potential
interaction with dentin sialophosphoprotein (DSPP) in human major
salivary glands. J Histochem Cytochem. 63:524–533. 2015. View Article : Google Scholar : PubMed/NCBI
|
5
|
Yamakoshi Y, Hu JC, Iwata T, Kobayashi K,
Fukae M and Simmer JP: Dentin sialophosphoprotein is processed by
MMP-2 and MMP-20 in vitro and in vivo. J Biol Chem.
281:38235–38243. 2006. View Article : Google Scholar : PubMed/NCBI
|
6
|
Suzuki S, Sreenath T, Haruyama N,
Honeycutt C, Terse A, Cho A, Kohler T, Müller R, Goldberg M and
Kulkarni AB: Dentin sialoprotein and dentin phosphoprotein have
distinct roles in dentin mineralization. Matrix Biol. 28:221–229.
2009. View Article : Google Scholar : PubMed/NCBI
|
7
|
Yang J, Kawasaki K, Lee M, Reid BM, Nunez
SM, Choi M, Seymen F, Koruyucu M, Kasimoglu Y, Estrella-Yuson N, et
al: The dentin phosphoprotein repeat region and inherited defects
of dentin. Mol Genet Genomic Med. 4:28–38. 2015. View Article : Google Scholar
|
8
|
Alvares K, Stern PH and Veis A: Dentin
phosphoprotein binds annexin 2 and is involved in calcium transport
in rat kidney ureteric bud cells. J Biol Chem. 288:13036–13045.
2013. View Article : Google Scholar : PubMed/NCBI
|
9
|
Fisher LW, Jain A, Tayback M and Fedarko
NS: Small integrin binding ligand N-linked glycoprotein gene family
expression in different cancers. Clin Cancer Res. 10:8501–8511.
2004. View Article : Google Scholar : PubMed/NCBI
|
10
|
Jain A, McKnight DA, Fisher LW, Humphreys
EB, Mangold LA, Partin AW and Fedarko NS: Small integrin-binding
proteins as serum markers for prostate cancer detection. Clin
Cancer Res. 15:5199–5207. 2009. View Article : Google Scholar : PubMed/NCBI
|
11
|
Anunobi CC, Koli K, Saxena G, Banjo AA and
Ogbureke KU: Expression of the SIBLINGs and their MMP partners in
human benign and malignant prostate neoplasms. Oncotarget.
7:48038–48049. 2016. View Article : Google Scholar : PubMed/NCBI
|
12
|
Ogbureke KU, Nikitakis NG, Warburton G,
Ord RA, Sauk JJ, Waller JL and Fisher LW: Up-regulation of SIBLING
proteins and correlation with cognate MMP expression in oral
cancer. Oral Oncol. 43:920–932. 2007. View Article : Google Scholar : PubMed/NCBI
|
13
|
Saxena G, Koli K, de la Garza J and
Ogbureke KU: Matrix metal-loproteinase 20-dentin
sialophosphoprotein interaction in oral cancer. J Dent Res.
94:584–593. 2015. View Article : Google Scholar : PubMed/NCBI
|
14
|
Rao RV, Hermel E, Castro-Obregon S, del
Rio G, Ellerby LM, Ellerby HM and Bredesen DE: Coupling endoplasmic
reticulum stress to the cell death program. Mechanism of caspase
activation. J Biol Chem. 276:33869–33874. 2001. View Article : Google Scholar : PubMed/NCBI
|
15
|
Denmeade SR and Isaacs JT: The SERCA pump
as a therapeutic target: Making a 'smart bomb' for prostate cancer.
Cancer Biol Ther. 4:14–22. 2005. View Article : Google Scholar : PubMed/NCBI
|
16
|
Mekahli D, Bultynck G, Parys JB, De Smedt
H and Missiaen L: Endoplasmic-reticulum calcium depletion and
disease. Cold Spring Harb Perspect Biol. 3:32011. View Article : Google Scholar
|
17
|
Raturi A, Ortiz-Sandoval C and Simmen T:
Redox dependence of endoplasmic reticulum (ER) Ca2+
signaling. Histol Histopathol. 29:543–552. 2014.
|
18
|
Giampietri C, Petrungaro S, Conti S,
Facchiano A, Filippini A and Ziparo E: Cancer microenvironment and
endoplasmic reticulum stress response. Mediators Inflamm.
2015:4172812015. View Article : Google Scholar : PubMed/NCBI
|
19
|
Wang M and Kaufman RJ: The impact of the
endoplasmic reticulum protein-folding environment on cancer
development. Nat Rev Cancer. 14:581–597. 2014. View Article : Google Scholar : PubMed/NCBI
|
20
|
Lemus L and Goder V: Regulation of
endoplasmic reticulum-associated protein degradation (ERAD) by
ubiquitin. Cells. 3:824–847. 2014. View Article : Google Scholar : PubMed/NCBI
|
21
|
Yadav RK, Chae SW, Kim HR and Chae HJ:
Endoplasmic reticulum stress and cancer. J Cancer Prev. 19:75–88.
2014. View Article : Google Scholar : PubMed/NCBI
|
22
|
Bertolotti A, Zhang Y, Hendershot LM,
Harding HP and Ron D: Dynamic interaction of BiP and ER stress
transducers in the unfolded-protein response. Nat Cell Biol.
2:326–332. 2000. View Article : Google Scholar : PubMed/NCBI
|
23
|
Brown JM and Giaccia AJ: The unique
physiology of solid tumors: Opportunities (and problems) for cancer
therapy. Cancer Res. 58:1408–1416. 1998.PubMed/NCBI
|
24
|
He B: Viruses, endoplasmic reticulum
stress, and interferon responses. Cell Death Differ. 13:393–403.
2006. View Article : Google Scholar : PubMed/NCBI
|
25
|
Martinon F: Targeting endoplasmic
reticulum signaling pathways in cancer. Acta Oncol. 51:822–830.
2012. View Article : Google Scholar : PubMed/NCBI
|
26
|
Moenner M, Pluquet O, Bouchecareilh M and
Chevet E: Integrated endoplasmic reticulum stress responses in
cancer. Cancer Res. 67:10631–10634. 2007. View Article : Google Scholar : PubMed/NCBI
|
27
|
Wang J and Sevier CS: Formation and
reversibility of BiP protein cysteine oxidation facilitate cell
survival during and post oxidative stress. J Biol Chem.
291:7541–7557. 2016. View Article : Google Scholar : PubMed/NCBI
|
28
|
Koumenis C: ER stress, hypoxia tolerance
and tumor progression. Curr Mol Med. 6:55–69. 2006. View Article : Google Scholar : PubMed/NCBI
|
29
|
Fu Y, Li J and Lee AS: GRP78/BiP inhibits
endoplasmic reticulum BIK and protects human breast cancer cells
against estrogen starvation-induced apoptosis. Cancer Res.
67:3734–3740. 2007. View Article : Google Scholar : PubMed/NCBI
|
30
|
Ye J, Kumanova M, Hart LS, Sloane K, Zhang
H, De Panis DN, Bobrovnikova-Marjon E, Diehl JA, Ron D and Koumenis
C: The GCN2-ATF4 pathway is critical for tumour cell survival and
proliferation in response to nutrient deprivation. EMBO J.
29:2082–2096. 2010. View Article : Google Scholar : PubMed/NCBI
|
31
|
Thorpe JA and Schwarze SR: IRE1alpha
controls cyclin A1 expression and promotes cell proliferation
through XBP-1. Cell Stress Chaperones. 15:497–508. 2010. View Article : Google Scholar
|
32
|
Livak KJ and Schmittgen TD: Analysis of
relative gene expression data using real-time quantitative PCR and
the 2(-Delta Delta C(T)) Method. Methods. 25:402–408. 2001.
View Article : Google Scholar
|
33
|
Joshi R, Tawfik A, Edeh N, McCloud V,
Looney S, Lewis J, Hsu S and Ogbureke KU: Dentin
sialophosphoprotein (DSPP) gene-silencing inhibits key tumorigenic
activities in human oral cancer cell line, OSC2. PLoS One.
5:e139742010. View Article : Google Scholar : PubMed/NCBI
|
34
|
Brunelle JK and Letai A: Control of
mitochondrial apoptosis by the Bcl-2 family. J Cell Sci.
122:437–441. 2009. View Article : Google Scholar : PubMed/NCBI
|
35
|
Heath-Engel HM, Wang B and Shore GC: Bcl2
at the endoplasmic reticulum protects against a Bax/Bak-independent
paraptosis-like cell death pathway initiated via p20Bap31. Biochim
Biophys Acta. 1823:335–347. 2012. View Article : Google Scholar
|
36
|
Wang X, Olberding KE, White C and Li C:
Bcl-2 proteins regulate ER membrane permeability to luminal
proteins during ER stress-induced apoptosis. Cell Death Differ.
18:38–47. 2011. View Article : Google Scholar
|
37
|
Nutt LK, Pataer A, Pahler J, Fang B, Roth
J, McConkey DJ and Swisher SG: Bax and Bak promote apoptosis by
modulating endoplasmic reticular and mitochondrial Ca2+
stores. J Biol Chem. 277:9219–9225. 2002. View Article : Google Scholar
|
38
|
Scorrano L, Oakes SA, Opferman JT, Cheng
EH, Sorcinelli MD, Pozzan T and Korsmeyer SJ: BAX and BAK
regulation of endoplasmic reticulum Ca2+: A control
point for apoptosis. Science. 300:135–139. 2003. View Article : Google Scholar : PubMed/NCBI
|
39
|
Nagelkerke A, Bussink J, Sweep FC and Span
PN: The unfolded protein response as a target for cancer therapy.
Biochim Biophys Acta. 1846:277–284. 2014.PubMed/NCBI
|
40
|
Corazzari M, Gagliardi M, Fimia GM and
Piacentini M: Endoplasmic reticulum stress, unfolded protein
response, and cancer cell fate. Front Oncol. 7:782017. View Article : Google Scholar : PubMed/NCBI
|
41
|
Marchi S and Pinton P: Alterations of
calcium homeostasis in cancer cells. Curr Opin Pharmacol. 29:1–6.
2016. View Article : Google Scholar : PubMed/NCBI
|
42
|
Lee E, Nichols P, Spicer D, Groshen S, Yu
MC and Lee AS: GRP78 as a novel predictor of responsiveness to
chemotherapy in breast cancer. Cancer Res. 66:7849–7853. 2006.
View Article : Google Scholar : PubMed/NCBI
|
43
|
de Ridder G, Ray R, Misra UK and Pizzo SV:
Modulation of the unfolded protein response by GRP78 in prostate
cancer. Methods Enzymol. 489:245–257. 2011. View Article : Google Scholar : PubMed/NCBI
|
44
|
Dong D, Ni M, Li J, Xiong S, Ye W, Virrey
JJ, Mao C, Ye R, Wang M, Pen L, et al: Critical role of the stress
chaperone GRP78/BiP in tumor proliferation, survival, and tumor
angiogenesis in transgene-induced mammary tumor development. Cancer
Res. 68:498–505. 2008. View Article : Google Scholar : PubMed/NCBI
|
45
|
Fu Y, Wey S, Wang M, Ye R, Liao CP,
Roy-Burman P and Lee AS: Pten null prostate tumorigenesis and AKT
activation are blocked by targeted knockout of ER chaperone
GRP78/BiP in prostate epithelium. Proc Natl Acad Sci USA.
105:19444–19449. 2008. View Article : Google Scholar : PubMed/NCBI
|
46
|
Daneshmand S, Quek ML, Lin E, Lee C, Cote
RJ, Hawes D, Cai J, Groshen S, Lieskovsky G, Skinner DG, et al:
Glucose-regulated protein GRP78 is up-regulated in prostate cancer
and correlates with recurrence and survival. Hum Pathol.
38:1547–1552. 2007. View Article : Google Scholar : PubMed/NCBI
|
47
|
Ren P, Chen C, Yue J, Zhang J and Yu Z:
High expression of glucose-regulated protein 78 (GRP78) is
associated with metastasis and poor prognosis in patients with
esophageal squamous cell carcinoma. OncoTargets Ther. 10:617–625.
2017. View Article : Google Scholar
|
48
|
Zhang J, Jiang Y, Jia Z, Li Q, Gong W,
Wang L, Wei D, Yao J, Fang S and Xie K: Association of elevated
GRP78 expression with increased lymph node metastasis and poor
prognosis in patients with gastric cancer. Clin Exp Metastasis.
23:401–410. 2006. View Article : Google Scholar : PubMed/NCBI
|
49
|
Kang J, Zhao G, Lin T, Tang S, Xu G, Hu S,
Bi Q, Guo C, Sun L, Han S, et al: A peptide derived from phage
display library exhibits anti-tumor activity by targeting GRP78 in
gastric cancer multidrug resistance cells. Cancer Lett.
339:247–259. 2013. View Article : Google Scholar : PubMed/NCBI
|
50
|
Toyoshima C, Nomura H and Sugita Y:
Crystal structures of Ca2+-ATPase in various
physiological states. Ann N Y Acad Sci. 986:1–8. 2003. View Article : Google Scholar : PubMed/NCBI
|
51
|
Roti G, Carlton A, Ross KN, Markstein M,
Pajcini K, Su AH, Perrimon N, Pear WS, Kung AL, Blacklow SC, et al:
Complementary genomic screens identify SERCA as a therapeutic
target in NOTCH1 mutated cancer. Cancer Cell. 23:390–405. 2013.
View Article : Google Scholar : PubMed/NCBI
|
52
|
Casemore D and Xing C: SERCA as a target
for cancer therapies. Integr Cancer Sci Ther. 2:100–103. 2015.
|
53
|
Dremina ES, Sharov VS, Kumar K, Zaidi A,
Michaelis EK and Schöneich C: Anti-apoptotic protein Bcl-2
interacts with and destabilizes the sarcoplasmic/endoplasmic
reticulum Ca2+-ATPase (SERCA). Biochem J. 383:361–370.
2004. View Article : Google Scholar : PubMed/NCBI
|
54
|
Axten JM, Medina JR, Feng Y, Shu A,
Romeril SP, Grant SW, Li WH, Heerding DA, Minthorn E, Mencken T, et
al: Discovery of
7-methyl-5-(1-{[3-(trifluoromethyl)phenyl]acetyl}-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine
(GSK2606414), a potent and selective first-in-class inhibitor of
protein kinase R (PKR)-like endoplasmic reticulum kinase (PERK). J
Med Chem. 55:7193–7207. 2012. View Article : Google Scholar : PubMed/NCBI
|
55
|
Bobrovnikova-Marjon E, Grigoriadou C,
Pytel D, Zhang F, Ye J, Koumenis C, Cavener D and Diehl JA: PERK
promotes cancer cell proliferation and tumor growth by limiting
oxidative DNA damage. Oncogene. 29:3881–3895. 2010. View Article : Google Scholar : PubMed/NCBI
|
56
|
Kanekura K, Ma X, Murphy JT, Zhu LJ, Diwan
A and Urano F: IRE1 prevents endoplasmic reticulum membrane
permeabili-zation and cell death under pathological conditions. Sci
Signal. 8:ra622015. View Article : Google Scholar
|
57
|
Shuda M, Kondoh N, Imazeki N, Tanaka K,
Okada T, Mori K, Hada A, Arai M, Wakatsuki T, Matsubara O, et al:
Activation of the ATF6, XBP1 and grp78 genes in human
hepatocellular carcinoma: A possible involvement of the ER stress
pathway in hepatocarcinogenesis. J Hepatol. 38:605–614. 2003.
View Article : Google Scholar : PubMed/NCBI
|
58
|
Dadey DY, Kapoor V, Khudanyan A, Urano F,
Kim AH, Thotala D and Hallahan DE: The ATF6 pathway of the ER
stress response contributes to enhanced viability in glioblastoma.
Oncotarget. 7:2080–2092. 2016. View Article : Google Scholar :
|
59
|
Zhao G, Kang J, Jiao K, Xu G, Yang L, Tang
S, Zhang H, Wang Y, Nie Y, Wu K, et al: High expression of GRP78
promotes invasion and metastases in patients with esophageal
squamous cell carcinoma. Dig Dis Sci. 60:2690–2699. 2015.
View Article : Google Scholar : PubMed/NCBI
|
60
|
Yuan XP, Dong M, Li X and Zhou JP: GRP78
promotes the invasion of pancreatic cancer cells by FAK and JNK.
Mol Cell Biochem. 398:55–62. 2015. View Article : Google Scholar
|
61
|
Oguma T, Ono T, Kajiwara T, Sato M,
Miyahira Y, Arino H, Yoshihara Y and Tadakuma T: CD4(+)CD8(+)
thymocytes are induced to cell death by a small dose of puromycin
via ER stress. Cell Immunol. 260:21–27. 2009. View Article : Google Scholar : PubMed/NCBI
|
62
|
Johnson GG, White MC, Wu JH, Vallejo M and
Grimaldi M: The deadly connection between endoplasmic reticulum,
Ca2+, protein synthesis, and the endoplasmic reticulum
stress response in malignant glioma cells. Neuro-oncol.
16:1086–1099. 2014. View Article : Google Scholar
|
63
|
Hammadi M, Oulidi A, Gackière F,
Katsogiannou M, Slomianny C, Roudbaraki M, Dewailly E, Delcourt P,
Lepage G, Lotteau S, et al: Modulation of ER stress and apoptosis
by endoplasmic reticulum calcium leak via translocon during
unfolded protein response: Involvement of GRP78. FASEB J.
27:1600–1609. 2013. View Article : Google Scholar : PubMed/NCBI
|
64
|
Michalak M, Milner RE, Burns K and Opas M:
Calreticulin. Biochem J. 285:681–692. 1992. View Article : Google Scholar : PubMed/NCBI
|