Development of skeletal muscle fibrosis in a rodent model of cancer cachexia.
Development of skeletal muscle fibrosis in a rodent model of cancer cachexia.
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DOI:
10.1002/cbf.3797
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发表时间:
2023-06
影响因子:
3.6
通讯作者:
Greene, Nicholas P.
中科院分区:
文献类型:
--
作者:
Washington, Tyrone A.;Schrems, Eleanor R.;Haynie, Wesley S.;Rosa-Caldwell, Megan E.;Brown, Jacob L.;Saling, Landen;Lim, Seongkyun;Perry Jr, Richard A.;Brown, Lemuel A.;Lee, David E.;Greene, Nicholas P.
Cachexia is characterized by losses in lean body mass and its progression results in worsened quality of life and exacerbated outcomes in cancer patients. However, the role and impact of fibrosis during the early stages and development of cachexia in under-investigated. The purpose of this study was to determine if fibrosis occurs during cachexia development, and to evaluate this in both sexes. Female and male C57BL6/J mice were injected with phosphate-buffered saline or Lewis Lung Carcinoma (LLC) at 8-week of age, and tumors were allowed to develop for 1, 2, 3, or 4 weeks. 3wk and 4wk female tumor-bearing mice displayed a dichotomy in tumor growth and were reassigned to high tumor (HT) and low tumor (LT) groups. In vitro analyses were also performed on cocultured C2C12 and 3T3 cells exposed to LLC conditioned media. Immunohistochemistry and quantitative polymerase chain reaction (qPCR) analysis were used to investigate fibrosis and fibrosis-related signaling in skeletal muscle. Collagen deposition in skeletal muscle was increased in the 1wk, LT, and HT groups in female mice. However, collagen deposition was only increased in the 4wk group in male mice. In general, female mice displayed earlier alterations in extracellular matrix (ECM)-related genes beginning at 1wk post-LLC injection. Whereas this was not seen in males. While overall tumor burden is tightly correlated to cachexia development in both sexes, fibrotic development is not. Male mice did not exhibit early-stage alterations in ECM-related genes contrary to what was noted in female mice.
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DOI:
10.1002/jcsm.12354
发表时间:
2018-10
期刊:
Journal of cachexia, sarcopenia and muscle
影响因子:
--
作者:
Brown JL;Lee DE;Rosa-Caldwell ME;Brown LA;Perry RA;Haynie WS;Huseman K;Sataranatarajan K;Van Remmen H;Washington TA;Wiggs MP;Greene NP
通讯作者:
Greene NP
DOI:
10.1002/jcsm.12232
发表时间:
2017-12
期刊:
Journal of cachexia, sarcopenia and muscle
影响因子:
--
作者:
Brown JL;Rosa-Caldwell ME;Lee DE;Blackwell TA;Brown LA;Perry RA;Haynie WS;Hardee JP;Carson JA;Wiggs MP;Washington TA;Greene NP
通讯作者:
Greene NP
DOI:
10.1152/ajpheart.00106.2015
发表时间:
2015-08-15
影响因子:
4.8
作者:
Devine, Raymond D.;Bicer, Sabahattin;Wold, Loren E.
通讯作者:
Wold, Loren E.
影响因子:
4.1
作者:
LIGHT, N;CHAMPION, AE
通讯作者:
CHAMPION, AE
影响因子:
5.6
作者:
Caja L;Dituri F;Mancarella S;Caballero-Diaz D;Moustakas A;Giannelli G;Fabregat I
通讯作者:
Fabregat I