Lamp2a is required for tumor growth and promotes tumor recurrence of hepatocellular carcinoma

Exploring the function of chaperone-mediated autophagy (CMA) in cancer has promoted progress in cancer treatment through the regulation of CMA pathways. However, CMA status and function in hepatocellular carcinoma (HCC) by focusing on the regulatory role of lysosome-associated membrane protein type...

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Published inInternational journal of oncology Vol. 49; no. 6; pp. 2367 - 2376
Main Authors Ding, Zhen-Bin, Fu, Xiu-Tao, Shi, Ying-Hong, Zhou, Jian, Peng, Yuan-Fei, Liu, Wei-Ren, Shi, Guo-Ming, Gao, Qiang, Wang, Xiao-Ying, Song, Kang, Jin, Lei, Tian, Meng-Xin, Shen, Ying-Hao, Fan, Jia
Format Journal Article
LanguageEnglish
Published Greece D.A. Spandidos 01.12.2016
Spandidos Publications
Spandidos Publications UK Ltd
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Abstract Exploring the function of chaperone-mediated autophagy (CMA) in cancer has promoted progress in cancer treatment through the regulation of CMA pathways. However, CMA status and function in hepatocellular carcinoma (HCC) by focusing on the regulatory role of lysosome-associated membrane protein type 2a (Lamp2a) remain to be clarified. We examined Lamp2a in a normal human liver cell line, 6 HCC cell lines, 10 normal liver samples as well as 42 HCC tissue and para-tumor tissues samples, and then validated it in 228 HCC patients to assess the relationship between Lamp2a and clinical prognosis. Gain and loss of Lamp2a function were also explored in HCC cell lines and xenograft models. Significantly lower level of Lamp2a expression was found in HCC cells and tissues compared with normal hepatic cells, para-tumor tissues and normal livers. Although no differences in HCC cell morphology or function were observed in relation to Lamp2a expression under normal culture or short-term starvation conditions, Lamp2a blockage significantly inhibited HCC cell viability under prolonged starvation. Critically, Lamp2a is required for HCC xenograft growth in vivo by helping cells to avoid apoptosis and promoting cell proliferation. Furthermore, a significant correlation between Lamp2a expression and tumor size or cumulative recurrence was uncovered in HCC patients. Collectively, the present study shows that impaired Lamp2a expression in HCC contributes to tumor cell viability and promotes tumor growth and recurrence. Targeting chaperone-mediated autophagy through Lamp2a may also imply a potentially novel treatment strategy for HCC.
AbstractList Exploring the function of chaperone-mediated autophagy (CMA) in cancer has promoted progress in cancer treatment through the regulation of CMA pathways. However, CMA status and function in hepatocellular carcinoma (HCC) by focusing on the regulatory role of lysosome-associated membrane protein type 2a (Lamp2a) remain to be clarified. We examined Lamp2a in a normal human liver cell line, 6 HCC cell lines, 10 normal liver samples as well as 42 HCC tissue and para-tumor tissues samples, and then validated it in 228 HCC patients to assess the relationship between Lamp2a and clinical prognosis. Gain and loss of Lamp2a function were also explored in HCC cell lines and xenograft models. Significantly lower level of Lamp2a expression was found in HCC cells and tissues compared with normal hepatic cells, para-tumor tissues and normal livers. Although no differences in HCC cell morphology or function were observed in relation to Lamp2a expression under normal culture or short-term starvation conditions, Lamp2a blockage significantly inhibited HCC cell viability under prolonged starvation. Critically, Lamp2a is required for HCC xenograft growth in vivo by helping cells to avoid apoptosis and promoting cell proliferation. Furthermore, a significant correlation between Lamp2a expression and tumor size or cumulative recurrence was uncovered in HCC patients. Collectively, the present study shows that impaired Lamp2a expression in HCC contributes to tumor cell viability and promotes tumor growth and recurrence. Targeting chaperone-mediated autophagy through Lamp2a may also imply a potentially novel treatment strategy for HCC.
Exploring the function of chaperone-mediated autophagy (CMA) in cancer has promoted progress in cancer treatment through the regulation of CMA pathways. However, CMA status and function in hepatocellular carcinoma (HCC) by focusing on the regulatory role of lyso-some-associated membrane protein type 2a (Lamp2a) remain to be clarified. We examined Lamp2a in a normal human liver cell line, 6 HCC cell lines, 10 normal liver samples as well as 42 HCC tissue and para-tumor tissues samples, and then validated it in 228 HCC patients to assess the relationship between Lamp2a and clinical prognosis. Gain and loss of Lamp2a function were also explored in HCC cell lines and xenograft models. Significantly lower level of Lamp2a expression was found in HCC cells and tissues compared with normal hepatic cells, para-tumor tissues and normal livers. Although no differences in HCC cell morphology or function were observed in relation to Lamp2a expression under normal culture or short-term starvation conditions, Lamp2a blockage significantly inhibited HCC cell viability under prolonged starvation. Critically, Lamp2a is required for HCC xenograft growth in vivo by helping cells to avoid apoptosis and promoting cell proliferation. Furthermore, a significant correlation between Lamp2a expression and tumor size or cumulative recurrence was uncovered in HCC patients. Collectively, the present study shows that impaired Lamp2a expression in HCC contributes to tumor cell viability and promotes tumor growth and recurrence. Targeting chaperone-mediated autophagy through Lamp2a may also imply a potentially novel treatment strategy for HCC.
Audience Academic
Author Zhou, Jian
Song, Kang
Fan, Jia
Liu, Wei-Ren
Wang, Xiao-Ying
Fu, Xiu-Tao
Shi, Ying-Hong
Peng, Yuan-Fei
Gao, Qiang
Jin, Lei
Tian, Meng-Xin
Shen, Ying-Hao
Ding, Zhen-Bin
Shi, Guo-Ming
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  givenname: Meng-Xin
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  givenname: Jia
  surname: Fan
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  organization: Liver Cancer Institute, Zhongshan Hospital, and Key Laboratory of Carcinogenesis and Cancer Invasion (Ministry of Education), Fudan University, Shanghai 200032, P.R. China
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Snippet Exploring the function of chaperone-mediated autophagy (CMA) in cancer has promoted progress in cancer treatment through the regulation of CMA pathways....
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StartPage 2367
SubjectTerms Animals
Apoptosis
Apoptosis - genetics
Autophagy
Autophagy - genetics
Carcinoma, Hepatocellular - pathology
Care and treatment
Cell growth
Cell Line, Tumor
Cell Movement - genetics
Cell Proliferation - genetics
Cell Survival - genetics
cell viability
chaperone-mediated autophagy
Development and progression
Gene expression
Genetic aspects
Glycoproteins
Health aspects
Hep G2 Cells
hepatocellular carcinoma
Hepatoma
Heterografts - growth & development
Humans
Hypoxia
Lamp2a
Liver cancer
Liver Neoplasms - pathology
Lysosomal-Associated Membrane Protein 2 - genetics
Lysosomal-Associated Membrane Protein 2 - metabolism
Medical prognosis
Mice
Mice, Nude
Neoplasm Recurrence, Local - genetics
Neoplasm Transplantation
Patients
Physiology
Prognosis
Proteins
RNA Interference
RNA, Small Interfering - genetics
Rodents
Studies
Transplantation, Heterologous
tumor recurrence
Title Lamp2a is required for tumor growth and promotes tumor recurrence of hepatocellular carcinoma
URI https://www.ncbi.nlm.nih.gov/pubmed/27840904
https://www.proquest.com/docview/1932331526
Volume 49
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