Colon cancer-associated transcript-1 enhances glucose metabolism and colon cancer cell activity in a high-glucose environment in vitro and in vivo
2020 Journal of Gastrointestinal Oncology. All rights reserved..
BACKGROUND: Our study aims to investigate the effect of colon cancer-associated transcript-1 (CCAT-1) on colon cancer cells' activity and metabolism under different glucose environments in vitro and in vivo.
METHODS: The levels of proliferation, migration, glucose, lactic acid, glucose metabolism-related enzymes, apoptosis genes, epithelial-mesenchymal transition (EMT) marker proteins, and PI3K/Akt/C-MYC pathway in CCAT-1-silenced SW620 cells cultured with different glucose levels were tested. Twenty BALB/C nude mice with hyperglycemia or normal blood sugar were transplanted with CCAT-1-silenced SW620 cells, blood glucose levels, lactic acid, insulin, and volume of transplanted tumor cells, the expression of EMT marker proteins, and PI3K/Akt/C-MYC pathway was detected.
RESULTS: The levels of proliferation, migration, glucose, lactic acid, LDH-A, PKM2, and HK2 decreased, apoptosis increased in SW620 cells cultured with low glucose or silenced CCAT-1 (P<0.05); levels of E-cadherin and ZO-1 significantly increased, and levels of N-cadherin, vimentin, and p-Akt decreased in CCAT-1-silenced SW620 cells cultured with high glucose (P<0.05). Hyperglycemic nude mice transplanted with CCAT-1-silenced colon cancer cells showed decreased tumor volume, blood glucose, lactic acid, insulin, P-AKT, and P-C-MYC than EV group (P<0.05).
CONCLUSIONS: CCAT-1 can enhance glucose metabolism and proliferation and migration of colon cancer cells by upregulating the expression of glycolysis enzymes, inhibiting apoptosis, activating the Akt/C-MYC pathway, and promoting EMT expression.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2020 |
---|---|
Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:11 |
---|---|
Enthalten in: |
Journal of gastrointestinal oncology - 11(2020), 6 vom: 30. Dez., Seite 1164-1185 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Cui, Ge [VerfasserIn] |
---|
Links: |
---|
Themen: |
C-MYC |
---|
Anmerkungen: |
Date Revised 19.04.2022 published: Print Citation Status PubMed-not-MEDLINE |
---|
doi: |
10.21037/jgo-20-474 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM320196070 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM320196070 | ||
003 | DE-627 | ||
005 | 20231225173049.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2020 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.21037/jgo-20-474 |2 doi | |
028 | 5 | 2 | |a pubmed24n1067.xml |
035 | |a (DE-627)NLM320196070 | ||
035 | |a (NLM)33456991 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Cui, Ge |e verfasserin |4 aut | |
245 | 1 | 0 | |a Colon cancer-associated transcript-1 enhances glucose metabolism and colon cancer cell activity in a high-glucose environment in vitro and in vivo |
264 | 1 | |c 2020 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Revised 19.04.2022 | ||
500 | |a published: Print | ||
500 | |a Citation Status PubMed-not-MEDLINE | ||
520 | |a 2020 Journal of Gastrointestinal Oncology. All rights reserved. | ||
520 | |a BACKGROUND: Our study aims to investigate the effect of colon cancer-associated transcript-1 (CCAT-1) on colon cancer cells' activity and metabolism under different glucose environments in vitro and in vivo | ||
520 | |a METHODS: The levels of proliferation, migration, glucose, lactic acid, glucose metabolism-related enzymes, apoptosis genes, epithelial-mesenchymal transition (EMT) marker proteins, and PI3K/Akt/C-MYC pathway in CCAT-1-silenced SW620 cells cultured with different glucose levels were tested. Twenty BALB/C nude mice with hyperglycemia or normal blood sugar were transplanted with CCAT-1-silenced SW620 cells, blood glucose levels, lactic acid, insulin, and volume of transplanted tumor cells, the expression of EMT marker proteins, and PI3K/Akt/C-MYC pathway was detected | ||
520 | |a RESULTS: The levels of proliferation, migration, glucose, lactic acid, LDH-A, PKM2, and HK2 decreased, apoptosis increased in SW620 cells cultured with low glucose or silenced CCAT-1 (P<0.05); levels of E-cadherin and ZO-1 significantly increased, and levels of N-cadherin, vimentin, and p-Akt decreased in CCAT-1-silenced SW620 cells cultured with high glucose (P<0.05). Hyperglycemic nude mice transplanted with CCAT-1-silenced colon cancer cells showed decreased tumor volume, blood glucose, lactic acid, insulin, P-AKT, and P-C-MYC than EV group (P<0.05) | ||
520 | |a CONCLUSIONS: CCAT-1 can enhance glucose metabolism and proliferation and migration of colon cancer cells by upregulating the expression of glycolysis enzymes, inhibiting apoptosis, activating the Akt/C-MYC pathway, and promoting EMT expression | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a C-MYC | |
650 | 4 | |a Colon cancer-related transcript-1 (CCAT-1) | |
650 | 4 | |a PI3K signaling pathway | |
650 | 4 | |a colon cancer | |
650 | 4 | |a glucose metabolism | |
650 | 4 | |a hyperglycemia | |
700 | 1 | |a Huang, Yuxuan |e verfasserin |4 aut | |
700 | 1 | |a Feng, Wenming |e verfasserin |4 aut | |
700 | 1 | |a Yao, Yunliang |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Hongchang |e verfasserin |4 aut | |
700 | 1 | |a Li, Xining |e verfasserin |4 aut | |
700 | 1 | |a Gong, Hui |e verfasserin |4 aut | |
700 | 1 | |a Liu, Jun |e verfasserin |4 aut | |
700 | 1 | |a Luo, Yifan |e verfasserin |4 aut | |
700 | 1 | |a Sun, Yandi |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Mengya |e verfasserin |4 aut | |
700 | 1 | |a Luo, Yan |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Ting |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Journal of gastrointestinal oncology |d 2010 |g 11(2020), 6 vom: 30. Dez., Seite 1164-1185 |w (DE-627)NLM209547685 |x 2078-6891 |7 nnns |
773 | 1 | 8 | |g volume:11 |g year:2020 |g number:6 |g day:30 |g month:12 |g pages:1164-1185 |
856 | 4 | 0 | |u http://dx.doi.org/10.21037/jgo-20-474 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 11 |j 2020 |e 6 |b 30 |c 12 |h 1164-1185 |