2019
DOI: 10.1016/j.ecoenv.2019.01.007
|View full text |Cite
|
Sign up to set email alerts
|

Adverse effects of bisphenol A on Sertoli cell blood-testis barrier in rare minnow Gobiocypris rarus

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

0
23
0
1

Year Published

2020
2020
2024
2024

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 43 publications
(24 citation statements)
references
References 50 publications
0
23
0
1
Order By: Relevance
“…Alternatively, the pollutants could have crossed the blood-testis barrier (BTB) and affected the actively dividing spermatogonia resulting in damaged DNA. The plausibility of this concept is low in conjunction with the fact that (1) the arterial blood flow to the testis is rather low (about 9.6 mL/min out of a cardiac output of~4.7 L/min) [49,50] and (2) the BTB is one of the tightest blood-tissue barriers known to exist in mammalian tissues, even more difficult to cross than the blood brain barrier [51][52][53]. In fact, one of the main role of the BTB is to prevent small molecules, and hence also harmful contaminants, from passing through the paracellular space [54].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Alternatively, the pollutants could have crossed the blood-testis barrier (BTB) and affected the actively dividing spermatogonia resulting in damaged DNA. The plausibility of this concept is low in conjunction with the fact that (1) the arterial blood flow to the testis is rather low (about 9.6 mL/min out of a cardiac output of~4.7 L/min) [49,50] and (2) the BTB is one of the tightest blood-tissue barriers known to exist in mammalian tissues, even more difficult to cross than the blood brain barrier [51][52][53]. In fact, one of the main role of the BTB is to prevent small molecules, and hence also harmful contaminants, from passing through the paracellular space [54].…”
Section: Discussionmentioning
confidence: 99%
“…In fact, one of the main role of the BTB is to prevent small molecules, and hence also harmful contaminants, from passing through the paracellular space [54]. On the other hand, despite being one of the strongest blood-tissue barriers, recent studies reported adverse effects of xenobiotics, such as bisphenol A and monobutyl phthalate, on Sertoli cell BTB [51,52]. To clarify this aspect, further investigation should be performed, particularly on spermatozoa, that unfortunately were not available to this study.…”
Section: Discussionmentioning
confidence: 99%
“…In colorectal cancer cells, mechanistic studies revealed conflicting results. Small interfering RNA (siRNA)-mediated silencing of TINCR in HCT116 and HCT8 cells suppressed cell proliferation, inhibited colony forming capacity and decreased cells migration and invasion [ 12 ]. On the other hand, another study in SW620 and HTC116 cells demonstrated the role of this lncRNA in suppression of proliferation and migration.…”
Section: Cell Line Studiesmentioning
confidence: 99%
“… Cancer type Targets/Regulators and Signaling Pathways Assessed cell lines Function Reference Gastric cancer STAU1, KLF2, CDKN2B/P15 and CDKN1A/P21 MGC803, BGC823, MKN45 and SGC7901, and the normal gastric epithelium cell line GES1 Δ TINCR: ↓ cell proliferation, ↓ colony formation, ↓ tumorigenicity, ↑ apoptosis ↑ TINCR: ↑ cell growth, ↑ cell cycle progression [ 6 ] E2F1/TINCR/STAU1/CDKN2B signaling axis MGC803, BGC823, MKN45, AGS, SGC7901 and GES-1 Δ TINCR: ↓ cell proliferation [ 11 ] HGC27, AGS, SGC-7901, MGC803 and GES-1 An approximately two-fold upregulated expression could be observed in GC cell lines for the lncRNAs TINCR. [ 10 ] miR-375/PDK1 KATO III, NCI-N87, HGC-27, and SNU-1 Δ TINCR: ↑ apoptosis, ↓ cell proliferation [ 4 ] Colorectal cancer miR‐7‐5p/PI3K/Akt/mTOR signaling pathway HCT116, HCT8, HT29, SW620 and SW480 ↑ TINCR: ↑ proliferation, ↑ migration, ↑ invasion [ 12 ] Wnt/β-catenin pathway LoVo, RKO, SW620, HCT116, SW480 and LS174T Δ TINCR: ↑ proliferation, ↑ migration, ↑ invasion [ 7 ] SW620 and HTC116 cells ↑ TINCR: ↓ proliferation, ↓ migration [ 13 ] Esophageal squamous cell carcinoma (ESCC) TE-13, KYSE-410, ECA-109, TE-1 and HEEC Δ TINCR: ↓ proliferation, ↓ migration, ↓ invasion, ↓ progression of cell cycle, ↑ apoptosis [ 22 ] …”
Section: Cell Line Studiesmentioning
confidence: 99%
See 1 more Smart Citation