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Detailed characterization of established STS PDX models.

Genomic profile, describing copy number gains and losses, obtained using low coverage whole genome sequencing of subsequent passages of STS PDX models, revealing a stable copy number profile throughout passaging. Copy number profile of (A) the MPNST model UZLX-STS39 and (B) the mesenchymal chondrosarcoma model UZLX-STS41.

Soft-tissue sarcomas (STS) represent a heterogeneous group of rare, malignant tumors of mesenchymal origin. Reliable in vivo sarcoma research models are scarce. We aimed to establish and characterize histologically and molecularly stable patient-derived xenograft (PDX) models from a broad variety of STS subtypes. A total of 188 fresh tumor samples from consenting patients with localized or advanced STS were transplanted subcutaneously in NMRI-nu/nu–immunodeficient mice. Once tumor growth was observed, the material was passaged to a next generation of mice. A patient-derived tumor sample was considered “successfully engrafted” whenever the sample was transplanted to passage 1. A PDX model was considered “established” when observing stable morphologic and molecular features for at least two passages. With every passage, histologic and molecular analyses were performed. Specific genomic alterations and copy-number profile were assessed by FISH and low coverage whole-genome sequencing. The tumor engraftment rate was 32% (61/188) and 188 patient samples generated a total of 32 PDX models, including seven models of myxofibrosarcoma, five dedifferentiated liposarcoma, five leiomyosarcoma, three undifferentiated pleomorphic sarcoma, two malignant peripheral nerve sheet tumor models, and single models of synovial sarcoma and some other (ultra)rare subtypes. Seventeen additional models are in early stages of engraftment (passage 1–2). Histopathologic and molecular features were compared with the original donor tumor and were stable throughout passaging. The platform is used for studies on sarcoma biology and suited for in vivo preclinical drug testing as illustrated by a number of completed and ongoing laboratory studies.

The NMDA subtype glutamate receptors (NMDARs) play important roles in both physiological and pathologic processes in the brain. Compared with their critical roles in synaptic modifications and excitotoxicity in excitatory neurons, much less is understood about the functional contributions of NMDARs to the inhibitory GABAergic neurons. By using selective NMDAR inhibitors and potentiators, we here show that NMDARs bidirectionally modulate the intrinsic excitability (defined as spontaneous/evoked spiking activity and EPSP-spike coupling) in inhibitory GABAergic neurons in adult male and female mice. This modulation depends on GluN2C/2D- but not GluN2A/2B-containing NMDARs. We further show that NMDAR modulator EU1794-4 mostly enhances extrasynaptic NMDAR activity, and by using it we demonstrate a significant contribution of extrasynaptic NMDARs to the modulation of intrinsic excitability in inhibitory neurons. Together, this bidirectional modulation of intrinsic excitability reveals a previously less appreciated importance of NMDARs in the second-to-second functioning of inhibitory GABAergic neurons.SIGNIFICANCE STATEMENTNMDA subtype of glutamate receptors (NMDARs) have important roles in brain functions, including both physiological and pathologic ones. The role of NMDARs in inhibitory neurons has been less elucidated compared with that in excitatory neurons. Our results demonstrate the importance of GluN2C/GluN2D-containing but not GluN2A/GluN2B-containing extrasynaptic NMDARs in modulating the intrinsic excitability of inhibitory neurons. These results further suggest distinct contributions of subsynaptic locations and subunit compositions of NMDARs to their functions in excitatory and inhibitory neurons. The above findings have implications for better understanding of brain diseases, such as schizophrenia.

Purpose: Oncogenic signaling in gastrointestinal stromal tumors (GIST) is sustained via PI3K/AKT pathway. We used a panel of six GIST xenograft models to assess efficacy of GDC-0941 as single agent or in combination with imatinib (IMA).Experimental Design: Nude mice (n = 136) were grafted bilaterally with human GIST carrying diverse KIT mutations. Mice were orally dosed over four weeks, grouped as follows: (A) control; (B) GDC-0941; (C) imatinib, and (D) GDC+IMA treatments. Xenografts regrowth after treatment discontinuation was assessed in groups C and D for an additional four weeks. Tumor response was assessed by volume measurements, micro-PET imaging, histopathology, and immunoblotting. Moreover, genomic alterations in PTEN/PI3K/AKT pathway were evaluated.Results: In all models, GDC-0941 caused tumor growth stabilization, inhibiting tumor cell proliferation, but did not induce apoptosis. Under GDC+IMA, profound tumor regression, superior to either treatment alone, was observed. This effect was associated with the best histologic response, a nearly complete proliferation arrest and increased apoptosis. Tumor regrowth assays confirmed superior activity of GDC+IMA over imatinib; in three of six models, tumor volume remained reduced and stable even after treatment discontinuation. A positive correlation between response to GDC+IMA and PTEN loss, both on gene and protein levels, was found.Conclusion: GDC+IMA has significant antitumor efficacy in GIST xenografts, inducing more substantial tumor regression, apoptosis, and durable effects than imatinib. Notably, after treatment withdrawal, tumor regression was sustained in tumors exposed to GDC+IMA, which was not observed under imatinib. Assessment of PTEN status may represent a useful predictive biomarker for patient selection. Clin Cancer Res; 19(3); 620–30. ©2012 AACR.

Introduction: The PI3K signaling pathway drives tumor cell proliferation and survival in gastrointestinal stromal tumor (GIST). We tested the in vivo efficacy of three PI3K inhibitors (PI3Ki) in patient-derived GIST xenograft models.Experimental Design: One hundred and sixty-eight nude mice were grafted with human GIST carrying diverse KIT genotypes and PTEN genomic status. Animals were dosed orally for two weeks as follows: control group (untreated); imatinib (IMA); PI3Ki (BKM120—buparlisib, BEZ235, or BYL719) or combinations of imatinib with a PI3Ki. Western blotting, histopathology, and tumor volume evolution were used for the assessment of treatment efficacy. Furthermore, tumor regrowth was evaluated for three weeks after treatment cessation.Results: PI3Ki monotherapy showed a significant antitumor effect, reflected in tumor volume reduction or stabilization, inhibitory effects on mitotic activity, and PI3K signaling inhibition. The IMA+PI3Ki combination remarkably improved the efficacy of either single-agent treatment with more pronounced tumor volume reduction and enhanced proapoptotic effects over either single agent. Response to IMA+PI3Ki was found to depend on the KIT genotype and specific model-related molecular characteristics.Conclusion: IMA+PI3Ki has significant antitumor efficacy in GIST xenografts as compared with single-agent treatment, resulting in more prominent tumor volume reduction and enhanced induction of apoptosis. Categorization of GIST based on KIT genotype and PI3K/PTEN genomic status combined with dose optimization is suggested for patient selection for clinical trials exploring such combinations. Clin Cancer Res; 20(23); 6071–82. ©2014 AACR.

Purpose:KIT aberrations were described in acral and mucosal melanomas in largely Caucasian populations. Asian populations are more prone to develop acral and mucosal than cutaneous melanomas, and may harbor a high frequency of KIT aberrations.Experimental Design: Melanoma subtypes (n = 502) were analyzed histologically to determine melanoma subtype. Tissue samples were analyzed for mutations in exons 9, 11, 13, 17, and 18 of KIT gene in genomic DNA by PCR amplification and Sanger sequencing. The copy numbers of the KIT gene were analyzed by quantitative PCR, and protein expression levels of KIT (CD117) were determined by immunohistochemistry.Results: The most common melanoma subtypes were acral (38.4%) and mucosal (33.3%) melanomas in this population. The overall incidence of somatic mutations within the KIT gene was 10.8% (54/502), and all subtypes of melanoma contained KIT mutations. Increases in KIT gene copy numbers were correlated to CD117 overexpression. The genetic mutations of KIT were unrelated to the age, gender, stage, thickness, and ulceration of primary melanomas. Importantly, the overall survival of melanoma patients with KIT mutations (P = 0.001) or with KIT aberrations (mutation plus amplification, P = 0.0002) was significantly shorter than that of patients without such alterations.Conclusion: In China, the prevalent melanomas are acral and mucosal melanomas. KIT mutations are detected in all melanoma subtypes. Our study suggests that increases in KIT gene copy numbers, but not KIT mutations, may be correlated to CD117 overexpression. For the first time, our study suggests that genetic KIT aberration is an adverse prognostic factor for melanoma. Clin Cancer Res; 17(7); 1684–91. ©2011 AACR.

PDF file - 566K, Xenograft tumor volume assessment, combined for all models. Tumor volume is expressed in percentage, as ratio between time point x baseline. Data are presented for all models (A), based on PTEN protein expression (B), and PTEN status by FISH (C). In GIST-PSW GDC-0941 treatment as single agent lasted 19 days (*). The dotted line shows the time of treatment withdrawal.

Table S2. Comparison in tumour volumes, proliferative and apoptotic activity between two weeks (end of treatment) and 5 weeks (end of regrowth experiment).

Supplemental Figures Legend

PDF file - 1222K, PTEN protein expression. Strong expression of PTEN was observed in GIST-DFR (A), GIST-BOE (B), GIST882 (C) and GIST48 (D). In GIST-PSW (E) and GIST882Ly (F) the majority of the tumor cells were PTEN negative, only scattered cells showed weak cytoplasmatic staining. The endothelium of blood vessels was used as internal positive control.

PDF file - 58K, Xenografts used in GDC-0941 efficacy experiments. All mice were subcutaneously transplanted with tumor fragment on both sides.

PDF file - 4757K, Western blotting showing KIT oncogenic signaling cascade. Three different tumor lysates were analyzed per treatment group.

Figure S1. Xenograft tumour volume assessment for the efficacy experiment. Tumour volume is displayed as percentage and normalized for baseline values and presented for UZLX-GIST3 (A), UZLX-GIST4 (B), UZLX-GIST2 (C), and GIST48 (D).

PDF file - 1683K, Representative micro-PET images from GIST-PSW (A) and GIST-DFR (B) mice treated with IMA or GDC+IMA are shown. Scans were perfromed at baseline, week four (end of the treatment) and weeks six and eight - during treatment discontinuation.

PDF file - 2344K, Representative images of control tumors from GIST882Ly (A-E) and GIST-DFR (F-J). The H&E staining was shown to illustrate tumor morphology (A, F). Expression of KIT (B, G), ANO1 (C, H), ETV1 (D, I) and CD44 (E, J) were studied to further characterize GIST xenograft models.

PDF file - 84K, Xenograft models characterization.

PDF file - 240K

Supplementary Figures S1-S8; Supplementary Tables S1-S3.

Purpose This study (NCT02083354) assessed the efficacy and safety of dabrafenib plus trametinib in East Asian patients with advanced BRAF V600-mutant cutaneous melanoma. Method Overall, 77 patients of East Asian origin (including 61 from Mainland China) with unresectable or metastatic BRAF V600-mutant cutaneous melanoma were enrolled. Prior treatment was allowed except with BRAF/MEK inhibitors. Patients received dabrafenib 150 mg twice daily and trametinib 2 mg once daily. The primary end-point was objective response rate (ORR) using Response Evaluation Criteria in Solid Tumours 1.1. Secondary end-points were duration of response (DOR), progression-free survival (PFS), overall survival (OS), pharmacokinetics and safety. Results At data cutoff (February 23, 2018; median follow-up, 8.3 months), treatment was ongoing in 36 patients (47%). The median age was 52 years; 32% of patients had elevated lactate dehydrogenase, and 84% had received prior systemic therapy. ORR was 61% (95% confidence interval: 49.2–72.0), with four patients (5%) achieving complete response. Median DOR and PFS were 11.3 and 7.9 months, respectively. Median OS was not reached. The most common adverse event (AE) of any grade was pyrexia (56%). Grade ≥III AEs occurred in 29 patients (38%). The most common grade ≥III AEs were pyrexia (8%) and anaemia (6%). AEs led to permanent discontinuation in five patients (6.5%). Mean Cmax for dabrafenib and trametinib was 3560 and 11.5 ng/mL (day 1) and 2680 and 27.1 ng/mL (day 15), respectively. Conclusion These results support the efficacy and tolerability of dabrafenib in combination with trametinib in East Asian patients with unresectable or metastatic BRAF V600-mutant cutaneous melanoma.

The tidal flat, located at the forefront of the coastal estuary wetland, serves as a peripheral defense line to maintain the stable ecological function of the estuary wetland. Therefore, the accurate identification of the stable state of a tidal flat is rendered as the decision-making basis for the restoration and management of estuary wetland ecosystems. Conducted at the tidal flat of the Liaohe Estuary Wetland, the study established a comprehensive evaluation index of tidal flat ecological stability (ECO-CSI) based on the Pressure-State-Response model and Rough Set theory. The driving factors and threshold values which affected the stability of the tidal flat were identified. The results showed that the average ECO-CSI value of the tidal flat during the past 30 years was 0.44 indicating, in general, a relatively stable state of the tidal flat. On the other hand, in 2017 the ECO-CSI value was 0.25, pointing that the tidal flat is in an unstable state currently. Among the factors affecting the tidal flat ecological stability, the artificial development activities were the major driving factors, and the urbanization and the traffic road scale were the key driving factors leading to the instability of the tidal flat. Of the natural factors, the sediment discharge, the flow in flood season, and the precipitation in the upstreams were the key guarantee factors for maintaining the material supply of the tidal flat. The threshold values for maintaining the ecological stability of the tidal flat in the Liaohe Estuary wetland were determined that the sediment discharge of the Liaohe River should be not less than 792.91 × 104t⋅y-1 and the scale of traffic roads in the tidal flat should be less than or equal to 770.9244 hm2. Hence, in the development and utilization of tidal flats and coastal wetlands, unreasonable human development activities should be minimized to avoid damage to the integrity and natural dispositions of the tidal flat. In this way, the stability of the tidal flat could be improved, contributing to the ecological security for the overall stability of the estuary wetland ecosystem.

In this article, polyaniline nanofibers (PANI-NF)/manganese dioxide composites (PANI/MnO2) were synthesized through an interfacial polymerization approach. The PANI-NF and MnO2 were obtained by in situ oxidation of aniline by potassium permanganate and in situ reduction of potassium permanganate by aniline, respectively. During the interfacial polymerization, the monomer aniline can only be oxidized to PANI after it diffuses into the water phase. This diffusion-control feeding process of the monomer results in nanofiber structure. The morphologies and crystal structures of the prepared PANI/MnO2 composites were measured by scanning electron microscopy and x-ray diffraction. The supercapacitive behaviours of these composites were analysed by cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) tests. The CV and GCD tests indicate that the PANI/MnO2 composites possess better electrochemical activity and higher capacitive properties compared to neat PANI nanofibers. The specific capacitance of PANI/MnO2 composites and PANI-NF are 751 F g−1 and 180 F g−1 at 0.2 A g−1 in Na2SO4 solution, respectively. We believe that the enhanced capacitive properties are related to the special nanostructure and strong interaction between PANI and MnO2 that resulted from the interfacial synthesis method.

Soft-tissue sarcomas (STS) represent a heterogeneous group of rare, malignant tumors of mesenchymal origin. Reliable in vivo sarcoma research models are scarce. We aimed to establish and characterize histologically and molecularly stable patient-derived xenograft (PDX) models from a broad variety of STS subtypes. A total of 188 fresh tumor samples from consenting patients with localized or advanced STS were transplanted subcutaneously in NMRI-nu/nu-immunodeficient mice. Once tumor growth was observed, the material was passaged to a next generation of mice. A patient-derived tumor sample was considered "successfully engrafted" whenever the sample was transplanted to passage 1. A PDX model was considered "established" when observing stable morphologic and molecular features for at least two passages. With every passage, histologic and molecular analyses were performed. Specific genomic alterations and copy-number profile were assessed by FISH and low coverage whole-genome sequencing. The tumor engraftment rate was 32% (61/188) and 188 patient samples generated a total of 32 PDX models, including seven models of myxofibrosarcoma, five dedifferentiated liposarcoma, five leiomyosarcoma, three undifferentiated pleomorphic sarcoma, two malignant peripheral nerve sheet tumor models, and single models of synovial sarcoma and some other (ultra)rare subtypes. Seventeen additional models are in early stages of engraftment (passage 1-2). Histopathologic and molecular features were compared with the original donor tumor and were stable throughout passaging. The platform is used for studies on sarcoma biology and suited for in vivo preclinical drug testing as illustrated by a number of completed and ongoing laboratory studies. ispartof: MOLECULAR CANCER THERAPEUTICS vol:18 issue:6 pages:1168-1178 ispartof: location:United States status: published

Summary: It has been proposed that sound information is separately streamed into onset and offset pathways for parallel processing. However, how offset responses contribute to auditory perception remains unclear. Here, loose-patch and whole-cell recordings in awake mouse primary auditory cortex (A1) reveal that a subset of pyramidal neurons exhibit a transient “Off” response, with its onset tightly time-locked to the sound termination and its frequency tuning similar to that of the transient “On” response. Both responses are characterized by excitation briefly followed by inhibition, with the latter mediated by parvalbumin (PV) inhibitory neurons. Optogenetically manipulating sound-evoked A1 responses at different temporal phases or artificially creating phantom sounds in A1 further reveals that the A1 phasic On and Off responses are critical for perceptual discrimination of sound duration. Our results suggest that perception of sound duration is dependent on precisely encoding its onset and offset timings by phasic On and Off responses.

Lateral posterior nucleus (LP) of thalamus, the rodent homologue of primate pulvinar, projects extensively to sensory cortices. However, its functional role in sensory cortical processing remains largely unclear. Here, bidirectional activity modulations of LP or its projection to the primary auditory cortex (A1) in awake mice reveal that LP improves auditory processing in A1 supragranular-layer neurons by sharpening their receptive fields and frequency tuning, as well as increasing the signal-to-noise ratio (SNR). This is achieved through a subtractive-suppression mechanism, mediated largely by LP-to-A1 axons preferentially innervating specific inhibitory neurons in layer 1 and superficial layers. LP is strongly activated by specific sensory signals relayed from the superior colliculus (SC), contributing to the maintenance and enhancement of A1 processing in the presence of auditory background noise and threatening visual looming stimuli respectively. Thus, a multisensory bottom-up SC-pulvinar-A1 pathway plays a role in contextual and cross-modality modulation of auditory cortical processing.

Studies on the influence of paper mill wastewater, which affects photosynthesis, on reed chlorophyll and biomass can provide a theoretical basis for the ecological restoration of wetland plants. The influence of different concentrations of wastewater (chemical oxygen demands (COD) of 300, 175 and 50 mg•L−1) and different irrigation times (germination, blade-expansion, rapid-growth, heading and maturity stages) on the contents of chlorophyll a, chlorophyll b, total chlorophyll and chlorophyll a/b in reeds were tested in experimental pools that simulated the wetland ecosystem of the Liaoning Shuangtai estuary. The contents of chlorophyll a, chlorophyll b, total chlorophyll and chlorophyll a/b all increased significantly with increasing concentrations of wastewater, and their contents all differed significantly from each other. The contents of chlorophyll a, chlorophyll b and total chlorophyll were maximal when irrigated at the beginning of all growth stages with COD of 300 mg•L−1(C1O) at 2.253, 0.458 and 2.711 mg•g−1 fresh weight (FW), respectively, with irrigation at the rapid-growth stage and were minimal in the control plants at 0.142, 0.068 and 0.210 mg•g−1 FW, respectively, with irrigation at maturity. Chlorophyll a/b was maximal at C1O at 5.753 with irrigation at germination stage and was minimal in the control plants at 2.113 with irrigation at maturity. Reed biomass was maximal at C1O at 3.26 kg, which was 2.76 times higher than the control. Reed biomass was positively correlated with the content of chlorophyll and with COD in the wastewater. Paper mill wastewater generally increased the content of chlorophyll and the net photosynthesis rate and enhanced the growth of reeds.

Physical education is an important part of teaching content, and basketball is an important part of physical education. Taking the effective way carries on the basketball sports training, may improve the student’s physical quality effectively. This paper first explains the concept of virtual reality technology and the necessity of simulation technology, and at the same time the application of virtual reality basketball teaching. And the research of fixed-point shooting based on virtual reality technology is discussed for readers’ reference.

In this paper, we demonstrate a simple approach to improve the electrochromic performances of polyaniline (PANI) by incorporating PANI nanofibers (PANI-NFs) synthesized by interfacial polymerization into water-soluble PANI:poly(styrene sulfonate) (PANI:PSS). The one-dimensional PANI-NFs endow spin-coated PANI film high electrochemical activities and electrochromic properties. The structures and morphologies of PANI-NFs were characterized by FTIR spectroscopy and SEM observation. The electrochemical behaviors of PANI/PANI-NFs composites were analyzed by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The electrochromic properties of composites were tested using electrochemical working station combining a UV-Vis spectrometer. The results show that the PANI-NFs with even diameter of ~ 30 nm can be synthesized easily using interfacial polymerization method. With the increasing of feeding amount of PANI-NFs, the oxidation peaks of CV curves shift to low potential direction, indicating enhanced electrochemical activities. The electrochromic test confirms that the PANI/PANI-NFs composites films have higher electrochromic contrast of 0.67 as comparison to 0.49 of PANI:PSS film. The PANI/PANI-NFs also exhibit excellent electrochromic stability. After 2000 cycles switching, only less than 4% contrast decay is observed. The enhanced electrochromic properties can be attributed to the small charge-transfer resistance and facile ion diffusion process brought by PANI-NFs. The EIS tests exhibit that with incorporating of highly conductive PANI-NFs, the PANI/PANI-NFs composites possess relatively lower charge-transfer resistance of 76 Ω as comparison to 94 Ω of neat PANI:PSS.

(1) Background: To reveal the intrinsic relationship between the tidal flat sediments in an estuary wetland and the runoff from the upstream river. This research was conducted in the tidal flats of the Liaohe estuary wetland. (2) Methods: The 137Cs and 210Pb dating technique was used to reconstruct the time correspondence between tidal flat sediments and runoff, and the periodic response was explored between the changes in the tidal flat sediments and runoff based on the spectrum analysis method. (3) Results: The average sedimentation rate in the tidal flat was 2.24 cm&middot, year&minus, 1 during the past 50 years. The amount of fine sediment particles deposited on the estuary tidal flat was directly related to the amount of sediments transported by the river and inversely proportional to the ability of rivers to transport fine matter. The high frequency reproduction cycle of 14&ndash, 15 years in the flood season flow and 5&ndash, 6 years in the annual sediment discharge of the Liaohe River correspond to the high and low frequency reproduction cycles of the median size of sediments in Liaohe estuarine wetland tidal flats. (4) Conclusions: The research clarified the hydrological constraints of the action law between Liaohe River runoff and the estuarine sediments. The periodic response between Liaohe River runoff and the sediment was established.

In this paper, the covalently bonded polyaniline (PANI) nanofiber/multi-walled carbon nanotubes (MWCNT) composites were synthesized via interfacial polymerization of aniline with para-phenylenediamine functionalized MWCNT at the interface of oil/water system. Owing to the diffusion-controlled growth process of PANI, PANI with uniform fiber structure were obtained. The morphology analysis showed that the diameter of PANI nanofiber decreased with the increasing of MWCNT loading amount. Impedance analysis showed that the charge-transfer resistances of the composites were reduced also with the increasing of MWCNT loading amount. The decreasing of charge-transfer resistances and change of morphology resulted in enhanced capacitive properties. Electrochemical tests showed that the specific capacitance of PANI, PANI/MWCNT-10% and PANI/MWCNT-20% were 405, 641 and 764 F·g-1, respectively. As comparison with pure PANI nanofiber, the specific capacitance of the composites increased by 58% and 88.6%, respectively.

Dedifferentiated liposarcoma (DDLPS) is a soft tissue malignancy characterized by amplification of the mouse double minute 2 homolog (MDM2) gene. MDM2 is a negative regulator of tumor protein 53 (TP53). We tested the in vivo efficacy of BI-907828, a small molecule inhibitor of the MDM2-TP53 interaction, in two DDLPS patient-derived xenografts (PDX). Partially immunodeficient mice were bilaterally engrafted with UZLX-STS3 (n = 24) and UZLX-STS5 (n = 24) human DDLPS tissue harboring MDM2 amplifications. Mice were grouped as follows: (a) vehicle (0.5% hydroxyethylcellullose) 10 ml/kg daily per os (p.o.); (b) doxorubicin 5 mg/kg weekly intraperitoneally (i.p.); (c) BI-907828 2.5 mg/kg daily p.o. and (d) BI-907828 10 mg/kg daily p.o. The treatment lasted for 15 days, all mice treated with BI-907828 were followed for 37 days post-treatment. Efficacy was assessed by tumor volume and histopathological evaluation. The 15-day treatment with 2.5 mg/kg and 10 mg/kg BI-907828 significantly inhibited tumor growth in UZLX-STS5 and -STS3 (p

The concentrations of dissolved copper in water of the Hun River were investigated to research the change characteristics of dissolved copper. We established the dynamic concentration function about time and spatial coordinate and convection diffusion equation of dissolved copper to obtain the distribution and accumulation characteristics of dissolved copper in the Hun River. In addition, we analyzed the advantages and disadvantages of two types of concentration functions of dissolved copper and used their own advantages to research the distribution and accumulation characteristics of dissolved copper in the Hun River. The results revealed the sources of copper pollution in water of the Hun River and provided theory basis to control copper pollution along the Hun River basin.